1779525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296661-G-A

1779525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296661-G-T

http://identifiers.org/hco/17/GRCh38#1779533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75296653-C-A

1779533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296653-C-T

1779978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296218-C-T

1781062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296028-G-T

1781066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296024-C-T

1781069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296021-A-G

http://identifiers.org/hco/17/GRCh38#1781076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75296014-C-A

1781076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296014-C-G

1781076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75296014-C-T

1781118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75295939-A-T

1781137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75295922-T-C

1781160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75295892-A-G

1781245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75295778-C-T

1781274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3 prime UTR variant
orthologous variants: 75295750-C-G

1781314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75295715-G-A

http://identifiers.org/hco/17/GRCh38#1781361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75295668-A-C

1781362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75295667-T-C

1781495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75295508-T-A

1781495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75295508-T-C

1781521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75295465-G-T

http://identifiers.org/hco/17/GRCh38#1781583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75295406-C-A

1781622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75295372-A-G

1781681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75295313-T-A

1781931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75295212-T-C

1782115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75295038-G-T

1782142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75295010-T-C

1782177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294975-G-A

1782177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294975-G-T

http://identifiers.org/hco/17/GRCh38#1782539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75294745-C-A

1782539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294745-C-T

1782593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294690-G-A

1782593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294690-G-T

1782597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294687-G-A

1782597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294687-G-T

1782686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294614-G-A

1782686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294614-G-T

1782730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294572-A-T

1782735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294567-A-T

1782989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294422-T-C

1783002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75294405-G-C

1783041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75294358-A-G

1783114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75294285-C-T

http://identifiers.org/hco/17/GRCh38#1783253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75294151-C-A

1783253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294151-C-T

1783255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294149-C-T

1783257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294147-C-T

1783295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294109-G-A

1783295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294109-G-C

1783364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75294045-G-C

1783444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75293965-G-A

1783529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 75293880-A-G

http://identifiers.org/hco/17/GRCh38#1783539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75293870-C-A

1783566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293845-G-A

1783566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293845-G-T

http://identifiers.org/hco/17/GRCh38#1783608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75293804-C-A

1783647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293774-T-C

1783666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293756-G-A

http://identifiers.org/hco/17/GRCh38#1783689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75293733-C-A

1783707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293715-T-G

1783715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293707-A-G

http://identifiers.org/hco/17/GRCh38#1783725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75293697-C-A

1783725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293697-C-G

http://identifiers.org/hco/17/GRCh38#1783726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75293696-A-C

http://identifiers.org/hco/17/GRCh38#1783749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75293664-C-A

1783749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293664-C-T

1783844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293568-G-T

1783845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293567-G-A

1783845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75293567-G-T

1783864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75293537-T-A

1783864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75293537-T-C

1783864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75293537-T-G

http://identifiers.org/hco/17/GRCh38#1783899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75293494-A-C

1783899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75293494-A-G

1783899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75293494-A-T

1783946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75293442-G-T

http://identifiers.org/hco/17/GRCh38#1783983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75293402-C-A

1783983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75293402-C-G

1783983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75293402-C-T

1784055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, undefined
orthologous variants: 75293335-G-A

1784134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, undefined
orthologous variants: 75293265-C-T

1784166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, undefined
orthologous variants: 75293235-C-T

1784304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, undefined
orthologous variants: 75293097-C-G

1784308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, undefined
orthologous variants: 75293093-G-A

1784470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75292933-G-A

1784487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75292916-T-C

1784508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75292896-C-G

1784544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75292864-T-C

http://identifiers.org/hco/17/GRCh38#1784586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75292824-C-A

1784586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75292824-C-T

1784744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75292690-G-C

1784749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75292685-T-C

1786353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75291643-A-G

1786374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75291625-T-C

1786405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75291609-G-T

1786486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75291547-T-C

1786516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75291521-T-C

1786817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75291262-G-T

1786932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75291147-T-C

1786937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75291142-T-A

1786944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75291135-C-T

http://identifiers.org/hco/17/GRCh38#1787020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75291061-A-C

1787020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75291061-A-G

1787064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290945-T-C

http://identifiers.org/hco/17/GRCh38#1787113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75290900-A-C

1787113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290900-A-G

1787115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290898-A-G

http://identifiers.org/hco/17/GRCh38#1787300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75290737-C-A

1787300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290737-C-T

1787318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290719-A-T

1787348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290689-G-C

http://identifiers.org/hco/17/GRCh38#1787393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75290636-C-A

1787393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290636-C-T

1787471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: synonymous variant
orthologous variants: 75290558-G-A

1787471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: synonymous variant
orthologous variants: 75290558-G-T

1787511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75290518-G-A

1787511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75290518-G-T

1787549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75290480-G-C

1787549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: synonymous variant
orthologous variants: 75290480-G-T

1787580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75290449-T-A

http://identifiers.org/hco/17/GRCh38#1787595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75290434-C-A

1787595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75290434-C-T

http://identifiers.org/hco/17/GRCh38#1787651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75290380-C-A

1787651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290380-C-T

http://identifiers.org/hco/17/GRCh38#1787722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75290309-C-A

1787722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290309-C-G

1787722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290309-C-T

1787736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290295-A-G

http://identifiers.org/hco/17/GRCh38#1787763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75290268-C-A

1787764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290267-G-A

1787907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290140-T-A

1787944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75290100-T-C

1788809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75289158-C-T

http://identifiers.org/hco/17/GRCh38#1789971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75288607-C-A

1789971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75288607-C-T

1790074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75288509-C-T

1791284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75287833-C-T

1791448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75287670-T-C

1791622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75287498-G-A

1792057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75287210-G-T

1792390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75286944-T-G

1792447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75286859-G-C

1792447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75286859-G-T

1797012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75284204-T-C

1799933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: synonymous variant
orthologous variants: 75281975-A-G

1799933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: synonymous variant
orthologous variants: 75281975-A-T

1799951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: synonymous variant
orthologous variants: 75281957-C-T

1799958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281950-G-A

1800084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281839-G-A

1800189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281734-C-T

1800205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281718-C-G

1800205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281718-C-T

http://identifiers.org/hco/17/GRCh38#1800333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75281587-A-C

1800333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: stop gained
orthologous variants: 75281587-A-T

1800394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281526-C-G

1800770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: synonymous variant
orthologous variants: 75281150-G-A

1800795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281125-T-C

1800831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281089-T-C

1800900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: missense variant
orthologous variants: 75281020-G-T

1801169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75280760-T-A

1801169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75280760-T-C

1801515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75280436-C-T

http://identifiers.org/hco/17/GRCh38#1801526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75280420-C-A

1801695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75280350-G-C

1801720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75280325-T-G

1801752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75280294-A-G

1803187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75279020-T-A

1803194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75279013-T-C

1804604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75278346-T-C

1804702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 75278248-G-C

1804738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278212-A-G

1804741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278209-G-A

http://identifiers.org/hco/17/GRCh38#1804746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75278204-A-C

http://identifiers.org/hco/17/GRCh38#1804821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75278144-A-C

1804821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278144-A-G

1804866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278106-T-A

1804866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278106-T-C

1804866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278106-T-G

1804924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75278055-T-C

1808362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275781-G-C

1808362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275781-G-T

1808495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275650-T-C

1810129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75273551-A-T

1811953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75273236-G-A

1811953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75273236-G-C

1811960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75273229-G-C

1812008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75273181-T-C

http://identifiers.org/hco/17/GRCh38#1812055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75273134-C-A

1812055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75273134-C-G

1812055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75273134-C-T

1812122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75273067-G-A

http://identifiers.org/hco/17/GRCh38#1812206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75272980-C-A

http://identifiers.org/hco/17/GRCh38#1812214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75272973-C-A

1812214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75272973-C-G

1827831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75240666-A-G

1827927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75240572-A-G

http://identifiers.org/hco/17/GRCh38#1827996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75240503-C-A

1827996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 75240503-C-T

1828011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75240488-A-G

1828011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75240488-A-T

1828029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75240467-G-A

http://identifiers.org/hco/17/GRCh38#1828044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75240452-C-A

1828044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75240452-C-G

1828044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75240452-C-T

1828069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75240427-A-G

1829128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75240011-T-C

1829128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75240011-T-G

http://identifiers.org/hco/17/GRCh38#1829153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75239997-C-A

1829280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239843-G-A

1829280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239843-G-T

1829370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239765-G-A

1829370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239765-G-T

1829393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239742-A-T

http://identifiers.org/hco/17/GRCh38#1829705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75239454-A-C

1829705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239454-A-T

1829712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239446-T-C

1829714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239444-T-C

1829716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75239442-G-T

1829730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75239428-G-A

1829730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75239428-G-T

1829837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75239343-T-A

1829837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75239343-T-C

1829837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75239343-T-G

1829848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75239332-T-A

1829848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75239332-T-C

1829903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75239279-G-A

1829903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75239279-G-T

1829911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75239271-T-G

1830200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238977-G-A

1830200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238977-G-C

1830200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238977-G-T

1830211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238966-G-A

1830211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238966-G-C

1830211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238966-G-T

1830260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238919-G-A

1830260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238919-G-T

1830357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238817-A-G

1830374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238802-C-T

1830381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238795-C-T

http://identifiers.org/hco/17/GRCh38#1830516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75238671-C-A

1830549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238636-G-A

1830549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238636-G-T

1830575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238608-T-C

http://identifiers.org/hco/17/GRCh38#1830579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75238604-C-A

1830579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21067
most severe consequence: intron variant
orthologous variants: 75238604-C-T