37858721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27628663-A-G

37858830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27628732-A-G

http://identifiers.org/hco/8/GRCh38#37858903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27628755-C-A

http://identifiers.org/hco/8/GRCh38#37858924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27628776-C-A

37858924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27628776-C-T

37859533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630004-A-G

http://identifiers.org/hco/8/GRCh38#37859536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27630007-C-A

37859536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630007-C-T

37859608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630079-G-T

37859625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630096-G-A

37859669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630142-T-C

37859671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630144-A-T

37859696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630177-T-C

http://identifiers.org/hco/8/GRCh38#37859703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27630185-C-A

37859703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630185-C-T

37859705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630187-G-A

37859705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630187-G-T

http://identifiers.org/hco/8/GRCh38#37859712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27630194-C-A

37859712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630194-C-G

37859714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630196-T-A

37859798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630312-G-A

37859798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630312-G-T

37859870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630371-A-G

37859935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630441-G-T

37860172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630679-A-G

37860217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630719-G-A

37860217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630719-G-T

37860301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27630779-A-G

37860980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27631124-G-T

37861026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27631175-C-T

http://identifiers.org/hco/8/GRCh38#37862210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27632494-C-A

37862210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632494-C-G

37862210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632494-C-T

http://identifiers.org/hco/8/GRCh38#37862211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27632495-C-A

37862217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632501-T-C

http://identifiers.org/hco/8/GRCh38#37862223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27632507-C-A

37862250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632535-G-T

37862273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632551-G-T

37862299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632575-T-C

http://identifiers.org/hco/8/GRCh38#37862323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27632599-C-A

37862323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632599-C-T

37862324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632600-T-C

37862425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27632848-C-G

http://identifiers.org/hco/8/GRCh38#37862513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27632921-C-A

http://identifiers.org/hco/8/GRCh38#37862745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27633092-C-A

37862769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27633117-G-A

37862769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27633117-G-T

http://identifiers.org/hco/8/GRCh38#37862795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27633139-C-A

37862795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27633139-C-T

37862809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27633153-T-A

37862843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27633183-A-G

37862844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27633184-G-T

37862893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 3 prime UTR variant
orthologous variants: 27633202-A-T

http://identifiers.org/hco/8/GRCh38#37862928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27633237-C-A

37862928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27633237-C-T

37862937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27633246-G-A

37863048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27633357-C-G

37863048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27633357-C-T

37863060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27633369-C-T

37863065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27633374-C-G

37863065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27633374-C-T

37866029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27637529-G-T

http://identifiers.org/hco/8/GRCh38#37869713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27639890-A-C

37869713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27639890-A-G

37869855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640014-G-A

37869856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640015-T-G

37870028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640196-G-A

37870222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640416-A-T

37870254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640445-T-C

37870254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640445-T-G

http://identifiers.org/hco/8/GRCh38#37870305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27640500-A-C

http://identifiers.org/hco/8/GRCh38#37870319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27640515-C-A

37870319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640515-C-G

37870319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640515-C-T

37870340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640564-G-T

http://identifiers.org/hco/8/GRCh38#37870369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27640653-C-A

37870369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640653-C-G

37870369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640653-C-T

37870381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640680-C-T

http://identifiers.org/hco/8/GRCh38#37870450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27640753-A-C

http://identifiers.org/hco/8/GRCh38#37870451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27640754-C-A

37870451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27640754-C-G

http://identifiers.org/hco/8/GRCh38#37870572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27640873-C-A

http://identifiers.org/hco/8/GRCh38#37870620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27640921-C-A

37870714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27641007-T-C

37870726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27641018-G-T

http://identifiers.org/hco/8/GRCh38#37870781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27641072-C-A

http://identifiers.org/hco/8/GRCh38#37871011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27641341-C-A

37871015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27641345-G-T

37871217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27641572-A-G

http://identifiers.org/hco/8/GRCh38#37871227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27641581-C-A

37871227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27641581-C-G

37871291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27641638-A-G

http://identifiers.org/hco/8/GRCh38#37871303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27641650-C-A

37871303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27641650-C-T

37871312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27641659-G-T

37871319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27641666-G-A

37871411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27641758-T-C

37871471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27641818-G-A

37871484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27641831-G-A

37871484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27641831-G-C

37871517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 27641864-T-A

37871673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 27641973-T-G

37871795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642070-A-G

37871801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642076-A-G

37871943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642197-G-A

37871943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642197-G-C

37871976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 27642230-C-T

37871994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642248-G-C

http://identifiers.org/hco/8/GRCh38#37872064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27642318-A-C

37872064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642318-A-G

http://identifiers.org/hco/8/GRCh38#37872087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27642338-C-A

37872087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642338-C-G

37872087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642338-C-T

37872128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642379-C-G

37872260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642475-C-T

37872297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642512-G-A

37872299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642514-G-C

37872325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642540-A-G

37872379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642594-C-G

37872379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642594-C-T

37872429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642644-C-T

37872453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642668-G-A

37872453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642668-G-T

37872464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642680-A-G

http://identifiers.org/hco/8/GRCh38#37872486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27642698-C-A

37872486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642698-C-T

37872488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642700-C-G

http://identifiers.org/hco/8/GRCh38#37872873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27642902-C-A

37872873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642902-C-T

http://identifiers.org/hco/8/GRCh38#37872936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27642956-C-A

37872936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27642956-C-T

37872968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27642985-T-C

http://identifiers.org/hco/8/GRCh38#37873258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27643253-C-A

37873258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27643253-C-T

37873585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27643381-G-A

37873594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27643390-A-G

37873761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27643531-T-C

http://identifiers.org/hco/8/GRCh38#37873786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27643556-C-A

37873910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27643613-A-G

http://identifiers.org/hco/8/GRCh38#37873922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27643625-A-C

37874008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27643700-A-G

37874234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27643906-T-C

37874243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27643915-C-T

37874427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27644085-T-C

37874428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27644086-G-A

37874428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27644086-G-T

http://identifiers.org/hco/8/GRCh38#37874433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#27644091-C-A

37874433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27644091-C-T

37874439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27644097-G-A

http://identifiers.org/hco/8/GRCh38#37874458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27644120-C-A

37874458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27644120-C-T

37874504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27644163-C-T

http://identifiers.org/hco/8/GRCh38#37874547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27644206-C-A

37874547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: 27644206-C-T

http://identifiers.org/hco/8/GRCh38#37874574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27644233-A-C

http://identifiers.org/hco/8/GRCh38#37874615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27644274-C-A

37874663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27644322-C-T

37874687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27644346-C-T

37874735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27644376-T-G

37874741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27644382-T-C

37874822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27644472-G-C

37874903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27644553-T-A

37874973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: 27644617-G-A

37874973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27644617-G-C

37875012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: 27644656-C-G

37875023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27644667-C-T

http://identifiers.org/hco/8/GRCh38#37875051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27644695-C-A

37875051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: 27644695-C-T

37875210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: 27644854-A-G

37875358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27644997-G-T

37875366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645005-G-T

37875397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645646-G-A

37875397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645646-G-T

37875409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645658-T-C

37875471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645680-G-A

37875471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645680-G-T

37875492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645701-A-G

37875542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645724-A-G

37875562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645744-C-T

37875604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645787-T-C

37875733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645907-A-G

37875767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27645941-T-A

http://identifiers.org/hco/8/GRCh38#37877099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27646245-A-C

37877099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27646245-A-G

37877113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: 27646259-C-T

37877120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27646266-G-A

37877120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27646266-G-C

37877143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: 27646289-A-G

37877156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: missense variant
orthologous variants: 27646302-T-G

37877458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: synonymous variant
orthologous variants: 27646604-G-A

37877572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27646716-G-T

37877585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27646729-A-G

http://identifiers.org/hco/8/GRCh38#37877595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27646739-C-A

37877595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27646739-C-G

37877595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27646739-C-T

37878153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27647324-A-G

37878164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27647335-C-T

37878175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27647346-T-A

http://identifiers.org/hco/8/GRCh38#37878272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27647370-C-A

http://identifiers.org/hco/8/GRCh38#37878289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27647387-C-A

37878289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27647387-C-T

37878319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27647408-G-A

37881128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27649533-C-T

http://identifiers.org/hco/8/GRCh38#37881508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27650004-C-A

37881508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27650004-C-T

37881603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27650093-G-A

37881665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27650152-G-C

37881799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27650174-T-C

37882868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27650621-T-C

37882893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27650636-T-C

37882962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27650699-A-G

37882963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27650700-A-G

37883606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27651849-C-G

37883606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27651849-C-T

37883737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27651992-C-T

37883794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27652039-G-A

37883794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27652039-G-T

37883834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27652078-T-C

37883857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27652101-A-G

http://identifiers.org/hco/8/GRCh38#37886297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27653592-C-A

37886297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27653592-C-T

37886605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27653847-A-G

37886665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27653916-T-C

37886770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27654001-T-G

http://identifiers.org/hco/8/GRCh38#37887169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27654351-A-C

37887182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27654364-G-A

37887296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27654495-C-T

37887649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27655073-C-T

37887734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27655159-G-A

http://identifiers.org/hco/8/GRCh38#37887846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27655267-A-C

37887846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27655267-A-G

37889490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27656329-G-A

37889498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27656337-T-C

37889751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27656588-A-G

37890159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27656704-C-G

37890218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27656781-T-C

37891369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27657691-A-G

37891873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27658297-T-C

37892058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27658474-G-A

37892085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27658500-C-T

37892107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, undefined
orthologous variants: 27658522-C-T

37893945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27660559-G-A

http://identifiers.org/hco/8/GRCh38#37894322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27660951-C-A

37894322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27660951-C-G

37894959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27661048-T-C

37895457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27661504-T-G

37895485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27661532-T-C

37895982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27662065-G-T

37896690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27662515-T-A

37896690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27662515-T-C

37896722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27662539-T-C

37896722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27662539-T-G

http://identifiers.org/hco/8/GRCh38#37896970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27662782-C-A

37897242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27662960-C-T

37897260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27662979-C-G

37897393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27663101-T-A

37897393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27663101-T-C

37897496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27663200-A-G

37897570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27663381-G-A

37897640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27663551-G-A

37897708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27663625-C-T

37897766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27663672-C-T

37897979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27663820-A-G

http://identifiers.org/hco/8/GRCh38#37898092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27663923-C-A

http://identifiers.org/hco/8/GRCh38#37898937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27664117-C-A

37898937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27664117-C-T

37898972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27664158-T-C

http://identifiers.org/hco/8/GRCh38#37899006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27664176-C-A

37899006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27664176-C-T

http://identifiers.org/hco/8/GRCh38#37899058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27664224-C-A

37899058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27664224-C-G

37899058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron variant
orthologous variants: 27664224-C-T

37899072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, splice_region_variant, stop_gained
orthologous variants: 27664238-G-A

37899072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 27664238-G-T

http://identifiers.org/hco/8/GRCh38#37899076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27664242-C-A

http://identifiers.org/hco/8/GRCh38#37899166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27664332-C-A

37899166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 27664332-C-G

37899166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 27664332-C-T

http://identifiers.org/hco/8/GRCh38#37899370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27664542-C-A

37899370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 27664542-C-T

http://identifiers.org/hco/8/GRCh38#37899405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27664577-C-A

37899405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 27664577-C-T

http://identifiers.org/hco/8/GRCh38#37899419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#27664591-C-A

37899443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30265
most severe consequence: 5 prime UTR variant
orthologous variants: 27664615-G-T