121567184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35448580-A-T

121567248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35448647-G-T

121567268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35448676-G-C

121567268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35448676-G-T

121567286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35448694-C-G

121567370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35448779-G-A

121567370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35448779-G-T

121567769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35449173-C-T

121568012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35449422-G-A

121568012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35449422-G-T

121568453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35449795-C-T

121568622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35449937-G-A

121568720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35450036-G-C

121568753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35450077-A-G

121568780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35450109-C-T

121568957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35450291-C-T

121569074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35450420-G-A

121569129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35450458-C-T

121569260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35450568-T-A

121569359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35450686-T-C

121571100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35451326-A-G

121571924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35452222-C-T

121572103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35452359-C-G

121572173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35452422-T-C

121572274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35452492-G-A

121572641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35452806-G-T

121572757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35452920-T-C

121572940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35453060-C-T

121573516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35453502-C-G

121573522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35453508-C-G

121573522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35453508-C-T

121573608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35453556-C-T

121573916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35453812-G-A

121574130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35454032-T-C

121574208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35454117-C-T

121575762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35455881-T-C

http://identifiers.org/hco/9/GRCh38#121575987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35456100-C-A

121575987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35456100-C-T

http://identifiers.org/hco/9/GRCh38#121575991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35456104-C-A

121575991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35456104-C-T

http://identifiers.org/hco/9/GRCh38#121576083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35456188-C-A

121576083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35456188-C-T

121576204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35456257-G-A

121576204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35456257-G-T

http://identifiers.org/hco/9/GRCh38#121576300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35456352-C-A

121576300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456352-C-T

121576315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456366-A-G

121576369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456399-A-G

121576379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456409-T-C

121576699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35456668-G-A

121576756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456712-G-A

121576756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456712-G-C

121576756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456712-G-T

121576807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456744-G-A

121577069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35456917-C-T

121577249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35457055-G-A

http://identifiers.org/hco/9/GRCh38#121577288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35457094-A-C

121577336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35457132-T-C

http://identifiers.org/hco/9/GRCh38#121577452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35457234-C-A

121577452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35457234-C-T

121577730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35457458-T-C

121578448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35457532-G-A

121579671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35457824-C-T

121581747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35458412-A-G

121581804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35458465-A-G

121581806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35458467-G-A

121582159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35458722-A-G

121582270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35458789-G-T

http://identifiers.org/hco/9/GRCh38#121582515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35459012-C-A

121586032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35461859-C-T

121586209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35462033-G-A

121586313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35462129-C-T

121586380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35462198-T-A

121586563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35462353-G-C

121587952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35463445-A-G

121587955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35463448-C-G

121587988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35463481-G-T

http://identifiers.org/hco/9/GRCh38#121587992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35463485-C-A

121588107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35463597-A-T

http://identifiers.org/hco/9/GRCh38#121588171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35463644-C-A

http://identifiers.org/hco/9/GRCh38#121588195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35463663-A-C

121589407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35464607-C-T

http://identifiers.org/hco/9/GRCh38#121589482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35464663-C-A

121589482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35464663-C-G

121589611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35464799-A-G

121589694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35464908-A-G

121591689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35466836-A-G

http://identifiers.org/hco/9/GRCh38#121592105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35467188-C-A

121592105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35467188-C-T

121592137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35467210-G-A

121592347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35467413-C-G

121592371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35467434-A-G

121592437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35467486-G-A

121592551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35467603-A-G

121592779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35467835-C-T

http://identifiers.org/hco/9/GRCh38#121592780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35467836-A-C

121592810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35467865-C-T

121594074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35468273-T-C

121594145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35468345-G-A

121594641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35468550-G-A

121594675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35468585-T-A

121594725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35468626-C-G

121596696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35470031-G-A

121596792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35470101-G-A

121596888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35470179-T-C

121597621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35471139-C-G

121597657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35471174-T-G

121597864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35471335-C-T

121597958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35471411-T-C

121598121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35471562-T-C

http://identifiers.org/hco/9/GRCh38#121598325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#35471764-C-A

http://identifiers.org/hco/9/GRCh38#121598331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#35471770-C-A

121598367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35471824-G-A

121598367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35471824-G-T

121598416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35471858-G-A

http://identifiers.org/hco/9/GRCh38#121598711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35472126-C-A

121598737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35472146-A-G

121598764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35472172-G-A

121598964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35472319-T-C

121598974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35472329-G-C

121598975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35472330-G-T

http://identifiers.org/hco/9/GRCh38#121599031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35472360-C-A

121599331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35472662-G-T

121599391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35472721-G-A

121599498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35472823-G-C

121599529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35472844-C-T

121599530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35472845-G-C

121599761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35473056-G-T

121600071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35473345-G-A

121600284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35473532-C-G

121600836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35473967-G-A

http://identifiers.org/hco/9/GRCh38#121601053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35474037-A-C

121601262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35474191-T-C

121601442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35474352-T-C

121601471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35474381-C-G

121601509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35474419-G-C

121601655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35474559-G-C

121601879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35474785-C-T

121601910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35474816-G-A

121603533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35475578-T-G

121604176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35475995-G-T

121604567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35476385-G-A

http://identifiers.org/hco/9/GRCh38#121604892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35476848-C-A

121604892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35476848-C-T

121605399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35477125-A-G

121605415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35477141-G-T

121605417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35477143-C-T

121605832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35477211-A-G

121607981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35478420-C-T

121608143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35478591-G-A

121608143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35478591-G-C

121608143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35478591-G-T

121608340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35478785-G-A

121608458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35478878-G-A

121608458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35478878-G-C

121608458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35478878-G-T

121608480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35478899-G-A

http://identifiers.org/hco/9/GRCh38#121608507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35478921-C-A

121608858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35479349-C-T

121609340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35479507-T-A

121609486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35479604-C-T

121609526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35479644-C-G

121609526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35479644-C-T

http://identifiers.org/hco/9/GRCh38#121609673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35479744-C-A

121610051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35480104-T-C

http://identifiers.org/hco/9/GRCh38#121610219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#35480271-A-C

121610329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35480384-A-G

121610571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35480580-T-C

121610787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35480739-G-C

121612332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35481322-A-G

121612381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35481385-G-A

121612852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35481751-A-G

121613053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35481953-G-C

121613550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35482424-C-T

121613554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35482428-T-G

121613563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35482442-C-T

121613640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35482522-G-A

121614231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35483021-A-G

121615101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35483188-T-C

121616102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35483939-T-C

121616297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35484107-G-A

121616495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35484298-G-A

121616511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35484301-T-G

121616599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35484374-G-A

121616631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35484403-G-A

121616722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35484473-G-C

121616722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35484473-G-T

121620130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35486983-G-A

121620443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35487246-C-T

121620780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35487522-C-G

http://identifiers.org/hco/9/GRCh38#121621002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#35487733-C-A

121621002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35487733-C-T

121621096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35487797-T-G

121622287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35488194-C-T

121622511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35488463-C-T

http://identifiers.org/hco/9/GRCh38#121622538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#35488490-C-A

121622538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35488490-C-T

121622548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35488500-C-T

121622908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35488852-G-A

121622908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35488852-G-T

http://identifiers.org/hco/9/GRCh38#121625876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35491152-C-A

121625885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35491163-G-A

121625903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35491174-C-G

121626036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35491281-C-T

121626306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35491497-G-A

121626443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35491647-A-G

121626443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35491647-A-T

121626522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35491741-C-T

121626971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492052-T-C

121627250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492367-C-T

121627295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492395-A-G

121627461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492526-A-G

121627470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492535-A-T

121627660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492852-T-C

121627755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492939-A-G

121627792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492975-T-C

121627810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35492989-C-T

121628006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35493168-C-T

121628285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35493596-T-C

121628290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35493601-T-C

121628290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35493601-T-G

121628345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35493644-G-A

121628512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35493763-G-A

121628512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35493763-G-T

121628597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35493841-T-A

121628917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35494134-T-C

121629034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35494223-G-A

121629482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35494568-G-A

121629550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35494636-T-C

121629743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35494791-G-T

121629912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35494920-C-T

121630070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35495079-T-C

121630311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35495272-G-A

121630743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35495540-G-T

121630781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35495585-T-C

121630994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35495763-A-G

http://identifiers.org/hco/9/GRCh38#121631184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35495934-C-A

121632020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496346-G-C

121632194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496483-C-T

121632257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496529-G-C

121632260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496532-G-A

121632298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496564-C-T

121632386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496651-G-T

121632407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496671-G-A

121632417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496681-C-G

121632456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496719-G-A

121632463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496726-T-C

121632486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496749-G-T

121632562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496821-T-C

121632660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35496896-G-A

121632904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35497117-C-G

http://identifiers.org/hco/9/GRCh38#121632975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35497342-C-A

121632975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35497342-C-T

121633197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35497567-T-C

121633542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35497899-G-C

121633610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35497967-G-A

121633918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35498411-T-C

121634743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499205-C-G

121634743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499205-C-T

http://identifiers.org/hco/9/GRCh38#121634894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35499266-C-A

http://identifiers.org/hco/9/GRCh38#121634991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35499345-C-A

121634991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499345-C-G

121634991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499345-C-T

121635032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499386-G-A

121635210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499583-T-C

121635210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499583-T-G

121635460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499811-T-C

121635593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35499923-A-T

121636854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35500610-T-G

121637532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35501101-T-C

http://identifiers.org/hco/9/GRCh38#121637661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35501212-C-A

121637724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35501280-G-C

121638260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35501549-A-G

121638574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35501749-C-T

121639156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35502349-T-C

121639396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35502562-A-T

121639579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35502746-C-T

121639673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35502803-T-C

121639859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35502933-C-G

121639906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35502980-T-C

121640266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35503315-G-T

121640270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35503319-G-A

121640330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35503350-C-T

121640475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35503477-G-A

http://identifiers.org/hco/9/GRCh38#121640678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35503680-C-A

http://identifiers.org/hco/9/GRCh38#121640844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35503827-A-C

121640887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35503851-T-C

121641081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35504017-T-A

http://identifiers.org/hco/9/GRCh38#121641140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35504075-C-A

121641141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35504076-T-C

121641156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35504091-G-T

121641246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35504179-G-A

121644830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35506019-A-G

121645337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35506503-C-T

http://identifiers.org/hco/9/GRCh38#121645685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35506769-A-C

121645719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35506788-C-T

http://identifiers.org/hco/9/GRCh38#121645857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35506887-C-A

121645857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35506887-C-G

121646532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35507524-G-C

121646624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35507616-C-T

121646789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35507767-T-G

121647031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35507960-T-C

121648603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35509234-T-C

121648826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35509453-G-A

121648949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35509657-G-C

121649347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35510044-C-G

121649437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35510140-C-G

121650547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35510807-C-G

121650554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35510814-T-A

121650593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35510852-C-T

121650956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35511253-A-G

121650996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35511293-C-T

121651283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35511708-G-A

121651438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35511818-C-G

121651438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35511818-C-T

http://identifiers.org/hco/9/GRCh38#121651658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35512054-C-A

121651658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35512054-C-T

121651784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35512180-G-A

121651784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35512180-G-T

121651980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512363-G-A

121651980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512363-G-C

121651980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512363-G-T

121651982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512365-A-G

121651982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512365-A-T

121651986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512369-T-C

121652035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512413-T-C

http://identifiers.org/hco/9/GRCh38#121652038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35512416-C-A

121652038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512416-C-T

121652506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35512848-G-T

121652741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513035-C-G

121652799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513070-C-T

121653063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513306-T-G

121653445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513385-G-A

121653577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513495-G-A

121653648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513530-T-A

121653714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513575-G-A

121653865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513717-G-A

121653865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513717-G-T

http://identifiers.org/hco/9/GRCh38#121653876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35513731-C-A

121653877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513732-G-A

121653877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513732-G-C

121653877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513732-G-T

121653948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35513806-T-C

121654510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35514222-G-C

121654917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35514501-A-G

121655833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35515330-T-C

121655843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35515339-A-G

http://identifiers.org/hco/9/GRCh38#121657225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35516531-A-C

121657269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35516577-C-T

121657449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35516744-A-G

http://identifiers.org/hco/9/GRCh38#121657668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35516920-A-C

121657763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517022-C-T

121657928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517173-G-A

121658052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517298-A-G

121658108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517350-C-T

121658148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517381-G-A

http://identifiers.org/hco/9/GRCh38#121658169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35517402-C-A

121658169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517402-C-T

121658420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517655-A-G

121658444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517679-C-T

121658712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35517928-G-T

121658807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35518005-C-T

121658897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35518094-G-A

121659009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35518196-A-G

121659097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35518278-C-T

121659159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35518320-G-A

http://identifiers.org/hco/9/GRCh38#121659196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35518356-A-C

121659268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35518417-G-A

121659268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35518417-G-T

121659948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35518769-A-G

121660328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35519081-A-G

121660430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35519155-G-A

121663035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35520097-A-G

121671398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35527112-T-C

121671415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35527129-C-G

121672046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35527753-G-T

121672181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35527889-G-A

121672215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35527924-A-G

121672655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35528341-A-T

121672970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35528572-C-T

121673094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35528703-A-G

http://identifiers.org/hco/9/GRCh38#121673410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35528948-C-A

121674896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35529671-G-T

121675032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35529819-G-A

121675201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35530031-G-A

121675529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35530334-G-A

121675797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35530627-C-T

121675836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35530666-G-T

121676236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35530973-T-C

121676310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35531047-C-G

121676310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35531047-C-T

121676448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35531145-G-T

121676576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35531257-G-A

121676639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35531316-A-G

121678120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35533412-C-T

121678171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35533463-C-T

121678223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35533510-A-G

http://identifiers.org/hco/9/GRCh38#121678229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35533516-C-A

121678629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35533856-G-T

121678718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35533940-T-C

121678898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35534117-T-C

121681331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35536602-A-T

121681581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35536846-C-T

121681674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35536943-G-C

121681833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35537111-A-G

121682105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35537316-C-T

http://identifiers.org/hco/9/GRCh38#121682475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35537595-C-A

121682553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35537668-C-T

121682564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35537679-A-G

121682597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35537712-A-G

121682878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35537904-G-A

121682880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35537906-A-G

121682971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35537956-G-T

121683085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538042-G-A

121683493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538354-G-A

121683545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538401-G-C

121683631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538484-T-C

121683642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538495-A-G

121683725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538589-T-A

121683725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538589-T-C

121683742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538611-G-C

121683896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35538752-C-T

121686749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35539617-T-A

121687030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35539894-G-C

121687333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35540160-G-T

121687382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35540204-T-G

121687438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35540260-G-T

121687447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35540269-C-T

121687620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35540441-G-A

121688164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35540895-G-A

121688263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35541509-A-G

121688470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35541712-C-T

121688811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35542028-G-A

121689455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35542287-A-G

121689538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35542364-C-G

121689645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35542435-G-A

http://identifiers.org/hco/9/GRCh38#121689934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35542668-A-C

121689936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35542670-C-T

121689977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35542707-G-A

121690445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35543080-G-T

121690498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35543119-T-C

121690651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35543274-A-G

121691012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35543583-A-G

121691332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35543819-G-C

121691469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35543942-C-T

121691562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35543961-C-T

121691654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35543988-C-T

121691795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35544105-C-G

121691832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35544125-G-A

121692007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35544294-G-T

121692279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35544427-A-G

121692461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35544612-A-G

121692511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35544666-G-C

121692653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35544870-G-A

121692967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35545109-G-A

121693096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35545233-G-A

121693310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35545362-C-T

http://identifiers.org/hco/9/GRCh38#121693409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35545432-C-A

121693409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35545432-C-T

121693424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35545445-G-A

121693677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35545690-G-A

121693678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35545691-G-C

121694196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35546048-T-C

121694268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35546129-G-A

121694950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35546724-T-G

121695089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35546857-C-T

121696132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35548227-G-A

121696320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35548341-C-T

121696328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35548349-C-T

121696608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35548558-G-A

121696790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35548693-G-T

121696853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35548740-T-G

121697281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35549177-C-G

121697386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35549233-C-T

121697511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35549299-T-C

121697740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35549648-T-A

121697799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35549706-C-G

121698020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35549947-C-G

121698020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35549947-C-T

121698123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35550009-T-C

http://identifiers.org/hco/9/GRCh38#121698670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35550926-C-A

121698701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35550941-G-T

http://identifiers.org/hco/9/GRCh38#121699376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35551555-C-A

121699376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35551555-C-G

121699376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35551555-C-T

http://identifiers.org/hco/9/GRCh38#121699475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#35551654-C-A

121699475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35551654-C-G

121699475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35551654-C-T

121699546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35551693-G-A

121699546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35551693-G-C

121699546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35551693-G-T

http://identifiers.org/hco/9/GRCh38#121699558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35551705-A-C

121699780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35551914-C-G

121699780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35551914-C-T

121700067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35552202-T-C

121701178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35553305-C-T

121701226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35553353-A-G

121701333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35553460-T-C

121701690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35553806-A-T

121701969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554046-C-T

121702006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554083-G-C

121702029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554104-T-A

121702154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554224-T-G

121702189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554259-G-C

121702482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554531-C-G

121702482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554531-C-T

121702692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554745-G-T

http://identifiers.org/hco/9/GRCh38#121702754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35554800-A-C

121702980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35554998-A-G

121703467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35555438-T-C

121703535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35555505-C-T

121703956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35555960-T-G

121704233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35556180-C-G

121704380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35556363-G-C

121704380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35556363-G-T

121704467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35556451-T-C

121704947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35556838-A-G

121705384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557288-A-T

121705533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557489-G-A

http://identifiers.org/hco/9/GRCh38#121705604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35557564-C-A

121705642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557599-A-G

121705791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557748-C-T

121705827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557778-G-C

121706032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35557979-T-G

121706271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35558205-G-A

121706556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35558471-A-G

121706752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35558636-C-G

121707080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35558916-C-T

121707081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35558917-G-A

121707199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35559021-G-C

121707467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35559334-G-A

121707474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35559349-G-A

121707554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35559444-G-C

121707588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35559483-C-G

121707962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35559858-T-C

121708248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35560124-C-G

121708267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35560143-A-G

121708386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35560279-A-T

121708548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35560540-C-T

121708754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35560733-C-G

121708950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35560888-G-A

121709000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35560935-C-T

121709136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561051-G-A

121709136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561051-G-C

121709248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561116-G-A

121709304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561163-C-T

121709351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561210-G-A

121709494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561326-C-T

121711019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561659-G-A

121711022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35561662-T-G

121711651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562210-G-T

121711655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562214-G-A

121711764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562316-C-G

121711784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562336-G-A

121711934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35562493-T-A

121712594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35563116-T-A

121712622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35563151-G-C

121714497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35564882-C-G

121714497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35564882-C-T

121714854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565151-G-T

121715069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565302-A-T

121715091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565325-G-A

121715118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565352-G-T

121715176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565396-T-A

121715749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565608-A-G

121715915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565748-G-T

121716132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35565963-C-G

http://identifiers.org/hco/9/GRCh38#121716192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35566018-C-A

121716612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566438-C-T

121716678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35566495-C-T

121718791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35568479-C-G

121718999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35568618-G-A

121719237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35568752-A-T

121719280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35568785-G-C

121719440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35568956-A-G

121719843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569275-G-A

121719950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569386-T-C

121720589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35569829-C-T

121721234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35570408-C-T

121721237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35570412-G-C

121721585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35570772-G-A

121721696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35570880-A-G

121721801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35570981-G-A

http://identifiers.org/hco/9/GRCh38#121722046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35571158-C-A

121722188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35571289-A-G

121723568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35572622-G-A

121723789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35572734-A-T

121724090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35572972-C-T

121724525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573482-C-G

121724556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573514-G-A

121724556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573514-G-C

121724714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573667-G-C

121724714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573667-G-T

121724798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35573721-C-T

121725063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35574060-G-A

121725063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35574060-G-T

121725081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35574078-G-A

121725162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35574152-T-C

121725164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35574154-C-T

121725166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35574156-C-T

121725167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35574157-G-A

121725277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35574264-G-A

121725364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35574349-C-T

121729180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35575150-A-G

121729419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35575375-C-T

121730006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35575956-G-A

121730006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35575956-G-T

http://identifiers.org/hco/9/GRCh38#121730018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35575968-C-A

121730106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576031-C-T

121730285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576206-T-G

121730474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576393-A-G

121730521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576407-G-A

121730993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35576699-A-T

http://identifiers.org/hco/9/GRCh38#121731024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35576730-C-A

121731408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35577095-T-C

121731525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35577222-G-A

121731525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35577222-G-C

121731646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35577306-G-A

121731794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35577423-T-G

121731880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35577509-A-G

121732060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35577669-G-A

121732310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35577882-T-C

121732469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35578039-C-T

121732701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35578183-A-G

121732884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35578325-A-G

121732901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35578342-A-G

121733175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35578570-C-G

121733175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35578570-C-T

121733276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35578670-T-A

121733539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35579184-T-C

121733745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35579379-G-T

121733948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35579505-A-G

121734603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35579687-G-A

121734695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35579817-G-A

121735167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35580238-G-A

121735167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35580238-G-C

121735296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35580332-T-C

121735507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35580421-T-C

121735621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35580494-C-T

121735656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35580530-C-G

121735706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35580587-A-G

121736110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35580939-G-T

121737077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35581862-C-G

121737202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35581974-A-G

121737236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35582008-G-A

121737265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35582031-G-A

121737265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35582031-G-C

121737518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35582237-G-A

121737751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582456-C-T

121737828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582523-G-A

121737933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582605-G-C

121738193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582837-G-A

121738341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35582951-T-C

121738399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583002-C-T

121738425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583029-T-C

121738844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583371-C-T

121739309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35583747-G-A

121739754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584291-G-A

121740402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584748-C-G

121740402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35584748-C-T

121740910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585143-A-G

121740994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585204-G-T

121741071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585251-C-G

121741071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585251-C-T

121741164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585310-C-T

121741225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585361-G-A

121741359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585483-G-C

121741496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585584-T-C

http://identifiers.org/hco/9/GRCh38#121741698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35585705-A-C

121741754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585760-C-G

121741777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35585778-C-T

121742886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35586067-C-T

121742907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35586088-G-T

121742941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586113-C-T

121742946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586118-T-C

121743078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586222-C-T

121743086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586230-G-A

121743102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586244-T-A

121743389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586531-G-A

http://identifiers.org/hco/9/GRCh38#121743447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35586578-C-A

121743447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586578-C-T

121743543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586672-G-A

121743612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35586743-C-T

121743812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35586901-G-C

121744968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35588066-T-G

121745573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35588501-G-A

121745573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35588501-G-C

121745620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35588534-T-G

121745877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35588727-T-G

121745953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35588791-A-G

121746998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35589762-T-C

121747136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35589850-G-A

121747782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35590167-G-C

121747909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35590257-C-T

121747953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35590295-C-T

121748080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35590375-T-C

121748293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35590564-G-A

121748382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35590629-G-A

121749061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35591116-C-T

121749130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35591185-C-G

121749198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35591249-C-T

121749264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35591283-T-A

121749326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35591333-T-C

121749891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35591699-G-C

121750845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35592687-A-G

121750946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35592786-G-T

121751108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35592858-T-C

121751132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35592872-C-T

121751249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35592927-G-A

121751249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35592927-G-T

http://identifiers.org/hco/9/GRCh38#121751261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35592951-C-A

121751322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35592995-G-A

121751322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35592995-G-C

121751322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35592995-G-T

121751350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35593024-C-T

121751372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35593046-G-T

121751423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593096-T-C

121751423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593096-T-G

121751516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593170-T-G

121751664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593233-G-T

http://identifiers.org/hco/9/GRCh38#121751669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35593238-C-A

121751669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593238-C-T

http://identifiers.org/hco/9/GRCh38#121751688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35593257-C-A

121751688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593257-C-T

121751788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35593351-T-G

http://identifiers.org/hco/9/GRCh38#121751850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35593412-C-A

http://identifiers.org/hco/9/GRCh38#121751880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35593440-C-A

121751895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35593448-A-G

http://identifiers.org/hco/9/GRCh38#121751911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35593465-C-A

121751911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35593465-C-G

121751911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35593465-C-T

121752053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593593-T-A

121752053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593593-T-C

121752307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35593805-G-A

121752556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35594036-G-A

121752647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35594132-G-T

121752682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35594154-T-C

121752908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35594362-G-T

http://identifiers.org/hco/9/GRCh38#121753827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35595422-C-A

121753827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35595422-C-T

121754054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35595626-G-A

121754129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35595701-T-C

121754178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35595751-A-T

121754248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35595819-G-T

121754298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35595870-G-T

121754611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596089-A-G

121755047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596530-T-C

121755128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596557-C-T

121755205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596655-C-G

121755342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596816-C-G

http://identifiers.org/hco/9/GRCh38#121755409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35596893-C-A

121755409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596893-C-G

121755409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596893-C-T

121755479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596964-G-A

121755479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35596964-G-T

121755539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35597022-G-C

http://identifiers.org/hco/9/GRCh38#121757127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35597774-C-A

121757127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 35597774-C-G

121757127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 35597774-C-T

121757243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35597874-G-A

121757264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35597890-T-A

121757291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35597925-G-C

121757291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35597925-G-T

121758132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35598203-G-A

http://identifiers.org/hco/9/GRCh38#121758248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35598311-A-C

http://identifiers.org/hco/9/GRCh38#121758386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35598405-C-A

121758386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35598405-C-T

121758587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35598578-G-T

121759126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35599059-G-A

121759126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35599059-G-T

http://identifiers.org/hco/9/GRCh38#121759428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35599401-C-A

http://identifiers.org/hco/9/GRCh38#121759770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35599715-C-A

121759770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35599715-C-T

http://identifiers.org/hco/9/GRCh38#121759783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35599732-C-A

121759965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35599910-G-A

121759965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35599910-G-T

121760169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35600114-G-A

121760175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35600120-C-T

121760220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35600165-C-T

121760316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35600261-T-C

121760473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600412-T-C

http://identifiers.org/hco/9/GRCh38#121760507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35600457-C-A

121760631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600561-A-G

121760656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600584-T-C

121760753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600632-A-G

121760759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600639-G-A

121760759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600639-G-C

121760763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600644-G-C

121760955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600787-T-C

121760982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600819-C-T

121761005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35600842-G-A

http://identifiers.org/hco/9/GRCh38#121761135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35600958-A-C

121761310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35601137-G-A

http://identifiers.org/hco/9/GRCh38#121761414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35601231-C-A

121761435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35601252-C-T

121761515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35601347-T-C

http://identifiers.org/hco/9/GRCh38#121763469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35602838-C-A

121763469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35602838-C-G

121763687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603066-A-G

121763802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35603185-C-T

121763896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603307-G-A

121763897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603308-G-A

121763901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603312-C-T

121763960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603377-A-T

121763967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603384-C-T

121763972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603387-C-T

121764085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603577-A-G

121764129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603618-G-A

121764145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603634-T-C

121764186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603667-C-G

121764186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603667-C-T

121764187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603668-C-T

121764490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603871-G-A

121764515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603882-A-G

121764576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603939-G-T

121764652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604012-C-G

121764652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604012-C-T

http://identifiers.org/hco/9/GRCh38#121764695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35604053-A-C

121764789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604115-C-G

121764873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604150-G-A

121764911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604159-C-T

121764918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604166-G-A

121765206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35604421-C-G

121765602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604582-A-T

121765913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604795-C-T

121766215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605058-T-A

121766221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605066-C-T

121766334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605143-C-G

121766416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605220-T-A

121766530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35605317-G-A

121766530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35605317-G-C

121766530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35605317-G-T

121766602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35605389-G-A

121766614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35605401-C-T

121766683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35605470-C-G

121766683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35605470-C-T

http://identifiers.org/hco/9/GRCh38#121766870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35605637-C-A

121766870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35605637-C-T

121766963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35605729-C-T

121767247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606210-C-T

121767391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606330-G-T

121767876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606700-C-T

121768229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606940-G-C

121768288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606994-A-G

http://identifiers.org/hco/9/GRCh38#121768305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35607003-C-A

121768305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35607003-C-G

121768305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35607003-C-T

121768340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35607021-G-A

121768340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35607021-G-T

121768416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35607067-A-G

121768483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35607134-T-C

121768980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35607638-C-T

121769004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35607675-A-T

121769072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35607740-C-T

121769562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35608159-A-G

121769794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35608256-G-A

121769794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35608256-G-T

121770001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35608434-T-A

121770215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35608648-G-A

121770215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35608648-G-T

121770419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35608708-G-A

121770419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35608708-G-T

121770707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: synonymous variant
orthologous variants: 35608933-T-C

121770710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: synonymous variant
orthologous variants: 35608936-G-A

http://identifiers.org/hco/9/GRCh38#121772478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35609761-C-A

121772478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35609761-C-T

121772481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35609764-C-G

121772485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35609768-G-A

121772485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35609768-G-C

121772485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35609768-G-T

121772515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35609796-G-A

121772515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35609796-G-T

121772833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: missense variant
orthologous variants: 35610091-G-A

121772833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: missense variant
orthologous variants: 35610091-G-T

121773261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: synonymous variant
orthologous variants: 35610519-T-A

http://identifiers.org/hco/9/GRCh38#121773309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35610567-A-C

121773309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: synonymous variant
orthologous variants: 35610567-A-G

121773309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: synonymous variant
orthologous variants: 35610567-A-T

http://identifiers.org/hco/9/GRCh38#121773536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35610778-C-A

http://identifiers.org/hco/9/GRCh38#121773622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35610861-C-A

121773622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35610861-C-T

121774005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35611101-G-A

121774506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35611534-G-A

121774506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35611534-G-T

121774512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35611540-G-C

121774569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35611567-G-A

121775131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35612033-C-G

http://identifiers.org/hco/9/GRCh38#121776175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35613017-C-A

121776175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613017-C-G

121776175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613017-C-T

121776180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613023-A-G

121776422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613260-A-G

121776531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613300-T-A

121776531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613300-T-G

121776535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613304-A-G

121777107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613655-G-A

121777321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35613852-A-T

121778077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35614389-C-T

121778119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35614440-G-A

121778326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35614610-T-C

121778639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35614988-A-G

121778766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35615109-C-T

http://identifiers.org/hco/9/GRCh38#121781641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35617606-C-A

121781641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35617606-C-T

121782062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: intron variant
orthologous variants: 35617844-C-G

http://identifiers.org/hco/9/GRCh38#121782680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35618345-C-A

121782680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618345-C-G

121782680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618345-C-T

http://identifiers.org/hco/9/GRCh38#121782753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35618442-C-A

121782753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618442-C-T

121782893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618573-G-T

121782931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618614-T-C

121782931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618614-T-G

121782932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618615-T-A

121782932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618615-T-C

121782932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618615-T-G

121782985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618620-T-C

121782985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618620-T-G

http://identifiers.org/hco/9/GRCh38#121783156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35618758-A-C

121783156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618758-A-G

121783229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618825-T-C

121783231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618827-G-A

121783231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618827-G-T

121783247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618843-G-A

121783282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618877-C-G

121783282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618877-C-T

http://identifiers.org/hco/9/GRCh38#121783283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35618878-A-C

121783283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35618878-A-G

http://identifiers.org/hco/9/GRCh38#121783697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35619281-C-A

121783697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35619281-C-T

121783820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35619401-T-C

121784044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35619610-G-A

121784044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35619610-G-T

http://identifiers.org/hco/9/GRCh38#121784244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35619776-C-A

121784287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35619811-A-G

121784394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35619932-G-A

121784553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620080-G-A

http://identifiers.org/hco/9/GRCh38#121784707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35620253-C-A

121784707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620253-C-G

121784707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620253-C-T

121784835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620379-G-T

121784912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620450-A-G

121784927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620465-G-A

121784927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620465-G-T

http://identifiers.org/hco/9/GRCh38#121785037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35620543-C-A

121785037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620543-C-G

121785037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620543-C-T

http://identifiers.org/hco/9/GRCh38#121785042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35620548-C-A

121785042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620548-C-G

121785042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620548-C-T

121785199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620689-C-G

121785199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620689-C-T

121785297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620781-A-G

121785314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620797-G-A

121785314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620797-G-T

http://identifiers.org/hco/9/GRCh38#121785315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35620798-C-A

121785315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620798-C-T

121785475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17294
most severe consequence: 3 prime UTR variant
orthologous variants: 35620951-T-A