17864425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: 41644389-A-G

17864425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: 41644389-A-T

17864437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: 41644401-C-G

17864437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: 41644401-C-T

http://identifiers.org/hco/8/GRCh38#17864445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41644409-A-C

17864445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: 41644409-A-T

http://identifiers.org/hco/8/GRCh38#17864516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41644474-A-C

17864516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: 41644474-A-G

17864532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: 41644490-T-C

17864532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3 prime UTR variant
orthologous variants: 41644490-T-G

17864588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 41644554-G-A

17864588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 41644554-G-C

17864648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: synonymous_variant, undefined
orthologous variants: 41644614-G-A

17864648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, undefined
orthologous variants: 41644614-G-C

17864679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41644645-G-T

17864715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 41644681-G-A

17864715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41644681-G-T

17864724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 41644690-T-G

17864730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 41644696-A-G

17864730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41644696-A-T

http://identifiers.org/hco/8/GRCh38#17864896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41644841-C-A

http://identifiers.org/hco/8/GRCh38#17865431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41646060-C-A

17865448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646077-G-C

17865448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646077-G-T

17865634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646263-G-C

17865634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646263-G-T

17865656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646284-A-G

17865656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646284-A-T

17865752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646552-A-G

17865807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646615-T-C

http://identifiers.org/hco/8/GRCh38#17865867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41646669-C-A

17865867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646669-C-G

17866163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646938-A-G

17866163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646938-A-T

17866171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41646949-C-T

17866361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647179-T-A

17866361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647179-T-C

17866361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647179-T-G

17866365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647183-T-A

17866581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647448-C-G

17866623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647490-T-A

17866655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647516-T-C

17866676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647538-C-T

17867015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41647841-C-G

http://identifiers.org/hco/8/GRCh38#17868276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41649127-C-A

http://identifiers.org/hco/8/GRCh38#17868318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41649150-C-A

17868318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41649150-C-G

17868322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41649154-G-C

17868322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41649154-G-T

17868357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649817-T-A

17868357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649817-T-C

17868357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649817-T-G

17868407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649870-G-A

17868407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649870-G-T

17868409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649872-A-G

http://identifiers.org/hco/8/GRCh38#17868435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41649898-A-C

17868435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649898-A-G

17868470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649923-A-G

17868470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649923-A-T

17868474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41649927-A-T

17868577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41650024-T-C

17868577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41650024-T-G

17868594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41650041-C-G

17868594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41650041-C-T

17868595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41650042-A-G

17868598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41650045-G-T

17868604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41650051-A-G

17868606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41650053-G-T

17868634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41650081-T-A

http://identifiers.org/hco/8/GRCh38#17868658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41650105-C-A

17868674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41650121-T-C

17868676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41650123-C-G

17868676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41650123-C-T

http://identifiers.org/hco/8/GRCh38#17868679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41650126-C-A

17868679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41650126-C-T

http://identifiers.org/hco/8/GRCh38#17868681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41650128-C-A

17868682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41650129-A-G

17868712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41650159-C-T

17868796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41650238-G-A

17868796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41650238-G-C

17868796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41650238-G-T

17868866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41650301-C-T

http://identifiers.org/hco/8/GRCh38#17868868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41650303-C-A

17868868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41650303-C-T

http://identifiers.org/hco/8/GRCh38#17868906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41650341-A-C

17868978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41650413-C-G

http://identifiers.org/hco/8/GRCh38#17869064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41650531-C-A

17869064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41650531-C-T

http://identifiers.org/hco/8/GRCh38#17869149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41650603-C-A

17869169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41650622-C-T

17869287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41650744-A-G

17872002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41651099-G-C

17872078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41651179-T-C

17872165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41651253-C-G

17872266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41651355-G-A

17873796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41652456-T-C

17873829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41652493-G-C

17873829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41652493-G-T

17873834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41652498-T-A

17873916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41652565-A-G

17873916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41652565-A-T

17873922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41652571-T-G

http://identifiers.org/hco/8/GRCh38#17874065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41652735-A-C

17874065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41652735-A-G

http://identifiers.org/hco/8/GRCh38#17874167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41652845-C-A

17874171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41652849-G-T

17874421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41653541-G-A

17874421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41653541-G-T

17874442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41653562-A-T

17874451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41653571-T-G

17874452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41653572-G-A

17874460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41653580-G-A

17874460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41653580-G-C

http://identifiers.org/hco/8/GRCh38#17874488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41653608-A-C

17874488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41653608-A-G

17874494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41653614-T-C

17874494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41653614-T-G

http://identifiers.org/hco/8/GRCh38#17874496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41653616-C-A

17874496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41653616-C-T

17874499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41653619-A-G

17874499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41653619-A-T

17874556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41653677-T-C

17874563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41653684-T-G

17874607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41653699-T-A

17874632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41653720-G-A

17874632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41653720-G-T

17874643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41653731-A-G

http://identifiers.org/hco/8/GRCh38#17874709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41653803-A-C

http://identifiers.org/hco/8/GRCh38#17874723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41653820-A-C

17874723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653820-A-G

17874732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653830-T-C

17874732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653830-T-G

http://identifiers.org/hco/8/GRCh38#17874736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41653834-A-C

17874736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653834-A-T

17874737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653835-T-A

17874737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653835-T-C

17874737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653835-T-G

17874766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653869-G-A

17874766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653869-G-C

17874766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653869-G-T

17874784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41653874-C-T

17874979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41654110-T-A

17874979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41654110-T-C

17874985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41654116-G-A

17874991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41654122-T-C

17875003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41654133-A-G

17875417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41654409-G-A

17876202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41654953-T-C

17876450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41655127-G-C

17876512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41655190-A-G

17876727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41655389-C-G

17877526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656084-C-T

17877539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656097-C-T

17877594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656152-C-T

17877837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656220-C-G

17877841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656224-T-C

17877885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656276-T-C

17877925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656309-T-C

17878286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656350-C-G

http://identifiers.org/hco/8/GRCh38#17878374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41656431-C-A

17878444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656491-C-T

17878462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656509-A-G

17878744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41656770-A-G

http://identifiers.org/hco/8/GRCh38#17878778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41656804-A-C

17878940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41657036-G-T

17879148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41657542-G-T

17879219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41657614-A-G

17879219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41657614-A-T

17879313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41657699-C-T

http://identifiers.org/hco/8/GRCh38#17879348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41657732-C-A

17879348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41657732-C-T

17880743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41661394-T-A

17880796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41661447-G-A

17880796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41661447-G-C

17881487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662220-T-C

17881500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662233-A-G

17881501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662234-T-C

17881501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662234-T-G

17881513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662248-A-T

17881742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662531-G-A

17881773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662565-G-T

http://identifiers.org/hco/8/GRCh38#17881815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41662588-C-A

17881815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662588-C-G

17881851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662616-T-A

17881851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662616-T-G

17882010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41662745-C-G

17882010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41662745-C-T

17882072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41662807-C-G

17882113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41662848-C-T

17882150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41662885-C-T

17882160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41662895-T-A

17882160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41662895-T-C

17882174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41662915-G-A

17882174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41662915-G-C

17882174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41662915-G-T

http://identifiers.org/hco/8/GRCh38#17882210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41662936-C-A

17882210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662936-C-T

17882238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41662963-T-G

17882307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41663031-G-A

17882307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41663031-G-T

17885380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41663353-C-T

http://identifiers.org/hco/8/GRCh38#17885541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41663513-A-C

17885541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41663513-A-G

http://identifiers.org/hco/8/GRCh38#17885726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41663637-C-A

17885726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41663637-C-G

17885726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41663637-C-T

17885747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41663671-G-A

17885747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41663671-G-C

17885747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41663671-G-T

http://identifiers.org/hco/8/GRCh38#17895315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#41667994-C-A

17895315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41667994-C-T

17895340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41668019-T-C

http://identifiers.org/hco/8/GRCh38#17895342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#41668021-C-A

http://identifiers.org/hco/8/GRCh38#17895343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41668022-A-C

17895343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41668022-A-G

17895355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41668034-T-C

17895379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41668058-T-C

17895402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41668084-A-G

17895425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41668107-G-A

17895489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41668162-C-G

17895641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, undefined
orthologous variants: 41668369-A-G

17895665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, undefined
orthologous variants: 41668393-C-G

17895693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41668425-G-A

17895693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41668425-G-C

17895693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41668425-G-T

17895735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41668551-G-T

17895826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41668691-C-G

17895826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41668691-C-T

17895928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41668801-A-T

17895973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, undefined
orthologous variants: 41668851-G-A

17895982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, undefined
orthologous variants: 41668860-G-A

17895982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, undefined
orthologous variants: 41668860-G-C

17896099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669163-T-A

17896099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669163-T-C

17896102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669166-A-G

17896107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669171-A-G

17896107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669171-A-T

17896189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669250-T-C

17896304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669360-G-A

17896304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669360-G-T

17896338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669395-G-A

17896338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669395-G-C

17896338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669395-G-T

http://identifiers.org/hco/8/GRCh38#17896345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#41669402-C-A

17896379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669436-T-C

17896408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669465-G-A

17896408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41669465-G-T

17896526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, undefined
orthologous variants: 41669581-T-C

17896546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669593-T-A

17896546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669593-T-C

17896546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669593-T-G

17896562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669609-T-C

17896562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669609-T-G

17896733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41669881-A-G

17896981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41670130-A-T

17897101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41670248-T-C

17897112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41670259-C-T

17897635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41672745-T-C

17897688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41672795-G-A

17899173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41674356-A-G

17899360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41674550-A-T

17899397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41674589-G-A

17899397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41674589-G-T

17899544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron variant
orthologous variants: 41674716-A-G

17900659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41677807-C-G

17900659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41677807-C-T

17900747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41677884-C-G

17900807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41677944-A-T

17900822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41677964-A-T

17903469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3695
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41678540-C-T