5897382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37394525-G-T

5897594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37394298-G-T

5897730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37394164-A-G

5897897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393986-G-A

5897897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393986-G-T

5898525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393444-G-A

5898525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393444-G-C

http://identifiers.org/hco/4/GRCh38#5898534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37393432-C-A

5898534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393432-C-T

5898542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393424-G-A

5898542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393424-G-T

5898608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393358-G-A

5898776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393200-A-G

5898780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393196-T-C

5898796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393180-T-C

5898986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393049-G-T

5898996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37393042-C-T

http://identifiers.org/hco/4/GRCh38#5899150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37392892-C-A

http://identifiers.org/hco/4/GRCh38#5899492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37392625-C-A

5899492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37392625-C-T

http://identifiers.org/hco/4/GRCh38#5899578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37392541-C-A

5899578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37392541-C-G

5899578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37392541-C-T

5899645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37392488-G-T

5899675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37392458-T-C

http://identifiers.org/hco/4/GRCh38#5899678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37392455-C-A

5899678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37392455-C-T

http://identifiers.org/hco/4/GRCh38#5899679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37392454-A-C

5899799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37392338-A-G

5900243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37391545-A-G

5900642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37391005-C-T

5900799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390887-A-G

5900834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390852-T-C

5900850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390836-T-G

http://identifiers.org/hco/4/GRCh38#5900923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37390778-C-A

5901024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390748-C-T

5901064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390708-A-G

http://identifiers.org/hco/4/GRCh38#5901069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37390703-C-A

5901276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390500-T-C

5901286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390490-G-A

5901488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390302-T-G

5901525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390265-A-G

5901588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390200-T-C

5901650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390144-G-A

5901650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390144-G-T

http://identifiers.org/hco/4/GRCh38#5901651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37390143-C-A

5901651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390143-C-T

5901653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390141-C-T

http://identifiers.org/hco/4/GRCh38#5901714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37390066-C-A

5901714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37390066-C-G

5901806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389992-G-A

5901808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389990-C-T

5901926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389843-A-G

http://identifiers.org/hco/4/GRCh38#5902034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37389777-C-A

5902034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389777-C-T

5902069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389765-C-T

http://identifiers.org/hco/4/GRCh38#5902142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37389667-C-A

5902159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389651-C-T

5902528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389243-G-A

5902530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389241-A-G

5902559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389213-C-T

5902596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389194-G-A

5902749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389060-A-G

5902749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37389060-A-T

http://identifiers.org/hco/4/GRCh38#5902758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37389054-C-A

http://identifiers.org/hco/4/GRCh38#5902998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37388840-C-A

5902998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388840-C-G

5903068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388781-C-T

5903079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388769-G-A

5903079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388769-G-T

5903133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388730-G-T

5903209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388656-T-A

5903215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388650-C-T

http://identifiers.org/hco/4/GRCh38#5903234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37388632-C-A

5903234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388632-C-T

5903312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388561-A-G

5903312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388561-A-T

5903361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388509-A-G

5903446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388432-T-C

http://identifiers.org/hco/4/GRCh38#5903482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37388408-C-A

http://identifiers.org/hco/4/GRCh38#5903485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37388405-A-C

5903518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388368-T-C

5903739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388169-T-C

5903740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388168-G-A

5903740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388168-G-T

http://identifiers.org/hco/4/GRCh38#5903975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37388006-A-C

5903975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37388006-A-G

5904001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387984-T-C

5904031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387954-T-C

5904139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387862-G-A

5904188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387816-T-C

5904212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387792-G-A

5904227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387777-T-C

5904227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387777-T-G

5904234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387770-G-A

http://identifiers.org/hco/4/GRCh38#5904356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37387688-C-A

5904356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387688-C-T

5904414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387618-G-A

5904414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387618-G-T

5904548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387402-A-T

5904671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387283-G-T

5904804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387168-C-T

http://identifiers.org/hco/4/GRCh38#5904828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37387146-A-C

5904828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387146-A-G

5904829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387145-G-C

5904838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387136-T-A

5904893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387091-A-G

http://identifiers.org/hco/4/GRCh38#5904930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37387055-C-A

5904961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37387030-G-A

http://identifiers.org/hco/4/GRCh38#5905126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37386874-A-C

http://identifiers.org/hco/4/GRCh38#5905191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37386831-C-A

5905352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37386694-G-T

http://identifiers.org/hco/4/GRCh38#5905512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37386536-A-C

5905512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37386536-A-G

5905532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37386516-A-G

5905591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37386480-A-T

5905777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37386318-G-A

5905817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37386275-A-T

5906749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37385536-T-C

5906807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37385473-T-A

5906807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37385473-T-G

5906939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37385346-A-G

5906989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37385299-T-C

5907270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37385038-G-A

5907275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37385033-A-G

5907399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384920-A-G

5907591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384729-G-T

5907689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384643-T-C

5907689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384643-T-G

5907729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384607-G-C

5907818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384545-C-T

5908090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384307-T-C

5908118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384281-G-T

5908174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384260-A-G

5908302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384206-T-G

5908497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384063-A-G

5908528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37384012-G-A

5908713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37383835-G-A

5908752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37383792-A-T

5908821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37383738-C-G

http://identifiers.org/hco/4/GRCh38#5909011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37383280-C-A

5909011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37383280-C-T

5909207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37383095-C-G

5910151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37382491-A-G

5910205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37382434-C-T

5910282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37382357-T-A

5910577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37382057-G-A

5911403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37380579-T-A

http://identifiers.org/hco/4/GRCh38#5911574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37380453-C-A

5911585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37380443-T-A

5911666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37380374-C-T

http://identifiers.org/hco/4/GRCh38#5912374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37380106-A-C

5912413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37380067-T-C

5912413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37380067-T-G

5912414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37380066-G-A

5912669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37379859-C-G

5912875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37379700-C-G

5913136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37379530-G-A

5913414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37379325-G-A

5914526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37378553-T-G

5915402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377867-G-A

5915664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377682-G-A

5915664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377682-G-C

5915683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377663-C-G

5915873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377614-T-G

5915934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377560-C-T

5915943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377547-T-C

5915990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377481-T-C

5916069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377402-T-C

5916362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377152-C-G

5916362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377152-C-T

5916436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37377081-C-T

5916667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37376907-A-G

5916821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37376777-C-T

5916853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37376750-T-A

5916950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37376667-A-G

5917070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37376584-A-G

5917285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37376225-G-A

5917764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372950-C-T

5917943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372770-C-G

5917960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372753-G-C

5918211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372552-T-C

5918262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372504-C-T

5918535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372343-A-G

5918536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372342-G-A

5918598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372281-A-T

5918678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37372180-C-T

5919008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371889-C-T

5921994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371638-C-T

5922029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371602-G-T

5922047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371586-A-G

5922122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371510-G-A

5922345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371320-T-C

5922386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371270-A-G

5922667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371128-G-A

5922752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37371114-C-T

5923358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37370557-G-T

5923398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37370509-A-G

5925362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37369481-G-T

http://identifiers.org/hco/4/GRCh38#5925752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37369043-C-A

5925787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37369027-C-G

5925810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37369009-C-T

5925823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37368997-G-C

5925863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37368958-G-C

5925863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37368958-G-T

5925993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37368847-G-A

5925998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37368842-T-G

5926165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37368704-G-A

5926204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37368671-G-T

5926208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37368667-G-T

5928042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37367630-T-G

5928052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37367620-C-T

5928053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37367619-G-A

5928241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37367435-C-T

5928300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37367374-C-G

5928514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37367188-C-T

5928646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37367088-T-C

5928646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37367088-T-G

5929088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37366720-C-T

5929242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37366570-C-T

5929243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37366568-G-A

5929538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37365151-G-A

5929549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37365140-G-A

5929611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37365085-A-G

5929824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37364898-T-A

5929886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37364842-C-G

5929896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37364834-T-C

5929908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37364822-C-T

5930091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37364675-A-G

5930410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37364432-T-C

5930725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37364130-A-G

5930757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37364098-C-T

http://identifiers.org/hco/4/GRCh38#5930973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37364016-A-C

5931035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37363954-G-A

5931035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37363954-G-T

5931087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37363917-C-T

5931088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37363916-G-A

5931260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37363732-A-G

5931276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37363716-C-T

5938582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37362697-G-A

5938687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37362584-C-T

5942775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360731-C-T

5942788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360718-C-T

5942813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360693-G-A

5943004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360521-A-G

5943016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360509-A-G

5943021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360504-T-C

5943120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360424-T-C

5943146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360405-T-A

5943176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360375-G-A

5945065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360085-T-A

5945083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37360065-T-C

http://identifiers.org/hco/4/GRCh38#5945156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37359998-C-A

5945190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37359964-G-A

5945259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37359894-G-A

5945259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37359894-G-T

5945438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37359717-G-A

5945448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37359652-G-C

5945505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37359594-T-C

http://identifiers.org/hco/4/GRCh38#5945538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37359560-C-A

5955259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37357323-T-C

5955264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37357318-G-A

5955302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37357278-G-A

5955318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37357267-A-T

http://identifiers.org/hco/4/GRCh38#5955391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37357190-A-C

5955682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37356748-C-G

5956578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37355841-A-G

5956673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37355781-T-C

5956738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355718-G-A

5956783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355675-T-C

5956851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355627-C-T

5956880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355599-G-T

5956922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355558-T-C

5956956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355512-G-T

5957003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355443-G-A

5957003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355443-G-C

5957003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355443-G-T

5957022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355424-T-C

http://identifiers.org/hco/4/GRCh38#5957042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37355400-C-A

5957072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355366-A-G

http://identifiers.org/hco/4/GRCh38#5957163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37355282-C-A

5957163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355282-C-T

5957182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355271-G-A

5957182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355271-G-T

5957238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355219-G-A

5957248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355209-A-G

5957273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355193-T-A

5957273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355193-T-C

5957278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355188-C-T

http://identifiers.org/hco/4/GRCh38#5957280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37355186-C-A

5957280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355186-C-T

http://identifiers.org/hco/4/GRCh38#5957355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37355136-C-A

5957355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355136-C-T

5957366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355134-T-C

http://identifiers.org/hco/4/GRCh38#5957406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37355086-A-C

http://identifiers.org/hco/4/GRCh38#5957415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37355077-C-A

5957421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355071-A-G

5957429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37355059-A-G

5957656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354969-G-A

5957701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354939-A-G

5957732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354900-T-C

5957733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354899-G-T

5957853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354817-A-G

5957891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354778-T-C

5957907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354764-A-G

http://identifiers.org/hco/4/GRCh38#5957955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37354720-A-C

5957955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354720-A-T

http://identifiers.org/hco/4/GRCh38#5958065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37354629-C-A

5958065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354629-C-T

5958082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354612-G-A

5958173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37354550-A-G

5959106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354465-G-A

5959108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354463-A-G

5959124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354448-G-T

http://identifiers.org/hco/4/GRCh38#5959197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37354389-C-A

5959197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354389-C-G

5959197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354389-C-T

5959226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354365-A-G

5959230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354361-A-G

5959251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354338-G-A

5959251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37354338-G-T

5959522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37354078-C-T

5959535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37354065-T-A

5959611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37353999-C-T

5959817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353838-T-C

5959818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353837-G-A

5959872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353783-C-T

5959895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353761-T-C

5959978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353695-C-G

5960190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353532-C-T

5960367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353353-T-C

5960432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353295-G-A

5960432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353295-G-C

5960438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353286-T-C

5960481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37353244-A-T

5963752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37352638-A-T

5963843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37352556-G-C

5963900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37352500-A-T

5963984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37352418-T-C

5964216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37352174-G-A

http://identifiers.org/hco/4/GRCh38#5964933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37351735-A-C

5964933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351735-A-G

5964933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351735-A-T

5964967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351701-G-T

5964968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351700-T-A

5964968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351700-T-C

5965014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351656-G-A

5965105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37351565-G-A

5965105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37351565-G-C

5965134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37351536-G-A

5965134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37351536-G-C

http://identifiers.org/hco/4/GRCh38#5965202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37351468-C-A

5965203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351467-A-G

5965230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351442-T-A

5965230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351442-T-C

5965295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351379-T-A

5965295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351379-T-C

5965295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351379-T-G

5965296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351378-G-A

5965296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351378-G-T

5965411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351300-G-T

5965645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351109-T-C

5965656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351098-C-T

5965722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351034-C-T

5965764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37351005-A-G

5967006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37350581-G-A

5967284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37350299-G-T

5967300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37350290-A-G

5967300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37350290-A-T

http://identifiers.org/hco/4/GRCh38#5967419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#37350190-A-C

http://identifiers.org/hco/4/GRCh38#5967420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37350189-A-C

5967459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37350150-T-C

http://identifiers.org/hco/4/GRCh38#5967563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37350056-C-A

5967563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37350056-C-T

http://identifiers.org/hco/4/GRCh38#5967579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37350040-C-A

5967579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37350040-C-T

http://identifiers.org/hco/4/GRCh38#5967595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37350025-C-A

5967595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37350025-C-T

5967650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349978-A-G

5967877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349763-C-T

5968095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349590-T-C

5968103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349582-C-T

5968258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349442-G-C

5968259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349441-T-A

5968372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349334-G-A

5968423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349296-G-T

5968471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37349246-A-G

5970989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37348114-G-A

http://identifiers.org/hco/4/GRCh38#5971294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37347826-C-A

5973026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37345170-T-C

5973117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37345091-G-C

5973133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37345075-C-T

5973156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37345050-C-G

5973156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37345050-C-T

5973167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37345039-C-T

5973446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344776-C-T

5973552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344699-G-A

5973552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344699-G-T

5973554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344697-G-A

5973554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344697-G-T

5973626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344629-G-A

5973640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344616-G-A

5973640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344616-G-C

5973640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37344616-G-T

http://identifiers.org/hco/4/GRCh38#5973659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37344597-C-A

5973659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 37344597-C-G

5973659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 37344597-C-T

5973660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 37344596-T-G

5973824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37344432-G-A

5973824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37344432-G-C

5973824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37344432-G-T

http://identifiers.org/hco/4/GRCh38#5973842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37344414-C-A

5973847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37344409-A-G

5973847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37344409-A-T

5975972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37343008-A-G

http://identifiers.org/hco/4/GRCh38#5980111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37339652-C-A

5980150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37339620-G-A

5980263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37339498-T-G

5980282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37339479-C-G

5980296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37339465-G-T

5980327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 37339434-T-A

5980327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 37339434-T-C

5980391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37339381-T-G

5980395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37339377-T-G

5980405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37339367-A-G

5980405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37339367-A-T

http://identifiers.org/hco/4/GRCh38#5980421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37339358-C-A

5980421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37339358-C-T

5980437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37339342-T-G

5980631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37338880-G-A

5980866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37338663-T-G

5980881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37338648-A-G

http://identifiers.org/hco/4/GRCh38#5981031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37338517-C-A

5981058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37338490-T-A

5981945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337631-T-A

http://identifiers.org/hco/4/GRCh38#5982023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37337561-C-A

5982023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337561-C-T

http://identifiers.org/hco/4/GRCh38#5982029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37337553-A-C

5982029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337553-A-G

5982053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337526-T-G

5982066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337513-T-C

5982323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337274-C-T

5982501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337165-C-T

5982610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337073-G-A

5982623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37337066-A-G

5982779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37336953-C-G

5982956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37336778-T-C

5982989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37336754-T-A

5982989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37336754-T-G

http://identifiers.org/hco/4/GRCh38#5982995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37336749-C-A

5983011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37336733-T-C

5983020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37336724-A-G

5983442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37336353-G-T

5983718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37336136-T-C

5983884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37335998-G-A

http://identifiers.org/hco/4/GRCh38#5983987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37335956-C-A

5984209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37335812-T-C

5984224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37335797-T-C

5984345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37335683-A-G

5984425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37335615-G-T

http://identifiers.org/hco/4/GRCh38#5984521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37335540-C-A

5984521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37335540-C-T

5988072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37333189-G-A

5988109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37333159-A-G

5988145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37333140-T-C

5988267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37333022-G-A

5988343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37332947-C-G

5988353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37332937-G-A

5988508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332788-G-A

5988508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332788-G-C

5988526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332770-G-A

5988526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332770-G-C

5988526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332770-G-T

5988577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332728-T-G

5988615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332690-A-G

5988665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332625-C-T

5988671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37332619-G-T

5988744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332558-C-T

5988773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37332529-G-A

5988773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332529-G-C

5988773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332529-G-T

5988897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332405-G-C

http://identifiers.org/hco/4/GRCh38#5988941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37332361-C-A

5988941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37332361-C-T

5988981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332321-T-A

5988981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332321-T-G

5988998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37332304-C-T

5989010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 37332292-G-T

5989061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37332241-T-C

5989082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37332220-C-T

http://identifiers.org/hco/4/GRCh38#5989181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37332121-A-C

5989181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37332121-A-G

5989181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332121-A-T

5989196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37332106-G-C

http://identifiers.org/hco/4/GRCh38#5989294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37332008-C-A

5989322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37331968-A-T

http://identifiers.org/hco/4/GRCh38#5989470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331838-C-A

5989470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331838-C-T

5989499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331809-C-G

http://identifiers.org/hco/4/GRCh38#5989500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331808-C-A

5989504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331801-C-T

5989526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331779-G-C

http://identifiers.org/hco/4/GRCh38#5989580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331728-C-A

5989580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37331728-C-T

5989670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37331638-C-G

5989670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37331638-C-T

5989715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37331599-T-C

5989728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331586-C-G

5989728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331586-C-T

5989750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331564-T-C

5989786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331534-G-C

5989809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331511-G-A

5989901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37331431-A-T

5989925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37331407-T-C

5989925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331407-T-G

http://identifiers.org/hco/4/GRCh38#5989975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331357-C-A

5989975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37331357-C-T

http://identifiers.org/hco/4/GRCh38#5990018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331317-A-C

5990018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37331317-A-G

http://identifiers.org/hco/4/GRCh38#5990088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331259-C-A

5990121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37331226-A-G

http://identifiers.org/hco/4/GRCh38#5990158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331189-C-A

5990171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37331176-C-T

http://identifiers.org/hco/4/GRCh38#5990229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331118-C-A

http://identifiers.org/hco/4/GRCh38#5990245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331102-C-A

5990245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37331102-C-T

http://identifiers.org/hco/4/GRCh38#5990265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37331082-C-A

5990265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37331082-C-G

5990316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37331031-T-A

5990316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37331031-T-C

5990345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37331002-A-G

5990404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330943-A-G

http://identifiers.org/hco/4/GRCh38#5990435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330912-C-A

http://identifiers.org/hco/4/GRCh38#5990467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330880-C-A

5990467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330880-C-T

5990469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330878-T-C

5990472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330875-A-G

5990472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330875-A-T

5990474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330873-G-A

5990479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330868-A-G

5990487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330860-C-T

http://identifiers.org/hco/4/GRCh38#5990491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330856-C-A

5990501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330846-G-A

5990503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330844-G-A

5990503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330844-G-T

http://identifiers.org/hco/4/GRCh38#5990511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330836-C-A

5990511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: stop gained
orthologous variants: 37330836-C-T

5990534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330813-G-A

5990537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330810-A-G

5990548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330799-A-G

5990548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330799-A-T

5990574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330773-T-G

5990576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330771-T-C

5990590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330757-G-A

5990590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330757-G-T

5990601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330746-A-G

5990604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330743-A-G

5990611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330740-G-T

5990612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330739-T-A

http://identifiers.org/hco/4/GRCh38#5990676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330671-A-C

5990676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330671-A-G

5990732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330615-G-T

5990740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330607-G-C

5990766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330581-G-T

5990782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330565-G-A

5990782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330565-G-T

5990804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37330543-G-A

5990804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330543-G-C

5990804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330543-G-T

5990808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37330539-G-T

http://identifiers.org/hco/4/GRCh38#5990831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330516-A-C

5990845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330502-T-C

http://identifiers.org/hco/4/GRCh38#5990889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330450-C-A

5990889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330450-C-T

5990937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330418-A-G

http://identifiers.org/hco/4/GRCh38#5990961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330405-C-A

5990961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330405-C-T

5990984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330382-T-C

5990999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330367-G-A

http://identifiers.org/hco/4/GRCh38#5991060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37330316-A-C

5991060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330316-A-G

5991176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330172-A-G

5991251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37330104-T-G

5991399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37329962-G-A

5991410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37329950-C-T

http://identifiers.org/hco/4/GRCh38#5991447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37329913-C-A

5991661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37329616-C-T

http://identifiers.org/hco/4/GRCh38#5991755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37329483-A-C

5992075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37329044-C-T

5992230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328885-G-C

5992268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328856-G-T

http://identifiers.org/hco/4/GRCh38#5992409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37328728-C-A

http://identifiers.org/hco/4/GRCh38#5992662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37328478-C-A

http://identifiers.org/hco/4/GRCh38#5992729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37328439-A-C

5992745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328422-G-A

http://identifiers.org/hco/4/GRCh38#5992779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37328389-C-A

5992786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328385-A-T

5992884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37328290-T-C

http://identifiers.org/hco/4/GRCh38#5992885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37328289-C-A

5992885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37328289-C-T

5993025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328172-A-G

http://identifiers.org/hco/4/GRCh38#5993038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37328159-C-A

5993038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328159-C-G

5993038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328159-C-T

5993073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328140-T-A

5993097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328117-G-A

5993166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328052-A-G

5993193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328034-G-A

5993193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328034-G-C

5993224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37328003-C-T

5993237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327990-T-C

5993247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327980-G-C

5993332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327895-G-A

5993332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327895-G-T

5993396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327841-A-G

5993432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327809-G-A

5994097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327582-G-A

5994097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327582-G-C

5994145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327538-G-T

http://identifiers.org/hco/4/GRCh38#5994211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37327484-C-A

5994211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327484-C-T

5994235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327462-G-A

5994243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327454-C-T

5994350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37327356-C-T

5994399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37327322-G-A

5994399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37327322-G-T

5994430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37327291-T-C

5994435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: synonymous variant
orthologous variants: 37327286-G-T

5994442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37327279-G-A

5994442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37327279-G-T

5994443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37327278-G-A

5994443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37327278-G-C

5994443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37327278-G-T

5994493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327229-G-A

5994493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327229-G-T

http://identifiers.org/hco/4/GRCh38#5994538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37327185-C-A

5994538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327185-C-T

5994539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327184-C-T

http://identifiers.org/hco/4/GRCh38#5994545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37327178-C-A

http://identifiers.org/hco/4/GRCh38#5994552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37327171-C-A

5994552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327171-C-G

5994552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327171-C-T

5994556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327167-T-A

5994556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327167-T-C

5994576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327142-T-A

5994576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327142-T-C

http://identifiers.org/hco/4/GRCh38#5994583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37327135-C-A

5994586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327132-A-G

5994611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327111-G-A

5994611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327111-G-T

5994639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327079-C-T

5994663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327062-C-G

5995180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37327278-G-A

5998423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37325055-T-C

5998508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37324984-G-A

5998508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37324984-G-C

5998520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37324972-G-A

5998535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37324959-A-G

5998604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37324903-A-G

5998781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37324708-C-G

5998781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37324708-C-T

5998838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37324639-T-A

5998998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37324512-T-C

5999052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37324468-G-A

5999251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37324258-A-T

5999390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37324094-A-T

5999490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37324032-C-T

6005427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37323515-T-C

6005428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37323514-T-C

6005581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37323374-G-A

6005658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37323306-T-C

6005695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37323281-G-T

6005700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37323276-C-T

http://identifiers.org/hco/4/GRCh38#6005741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37323233-A-C

6006121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37322979-C-T

6006201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37322904-A-G

6006346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37322740-G-A

6006542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37322519-A-T

6007393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37321837-G-C

6007432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37321797-A-T

6007914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37320911-A-G

6007961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37320862-A-G

6008030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: 37320811-A-G

6008194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: 37320647-T-G

http://identifiers.org/hco/4/GRCh38#6008226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37320615-C-A

6008226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: 37320615-C-T

6008232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 37320609-G-A

6008232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: 37320609-G-T

6008234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: 37320607-G-C

http://identifiers.org/hco/4/GRCh38#6008244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#37320597-C-A

6008262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: 37320582-C-T

6008442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 37320363-G-A

6008442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 37320363-G-C

6008442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 37320363-G-T

6008450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: 37320355-A-G

6008466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant
orthologous variants: 37320339-G-A

http://identifiers.org/hco/4/GRCh38#6008484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37320321-A-C

6008484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 37320321-A-G

http://identifiers.org/hco/4/GRCh38#6008488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37320317-C-A

6008522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 37320292-T-C

http://identifiers.org/hco/4/GRCh38#6008526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37320288-C-A

6008540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 37320274-T-C

6008613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37320205-A-G

6008635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37320183-G-T

6008756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37319922-G-C

6008838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37319846-G-A

http://identifiers.org/hco/4/GRCh38#6009059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37319639-C-A

6009151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37319547-C-G

6009331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37319409-G-A

6009395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37319345-A-G

6009467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37319278-G-C

http://identifiers.org/hco/4/GRCh38#6009535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37319218-A-C

6009814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37318940-G-A

6009925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37318755-C-T

6010128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37318555-A-G

6010218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37318472-C-T

6010506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37318200-T-C

6010524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37318183-T-G

6010551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37318156-G-A

6010738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37318034-T-C

6010806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317977-G-A

6010894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317885-T-C

6010908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317871-C-G

6010915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317864-A-G

6011022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317762-G-C

http://identifiers.org/hco/4/GRCh38#6011258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37317648-C-A

6011258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317648-C-G

http://identifiers.org/hco/4/GRCh38#6011274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37317633-C-A

6011274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317633-C-T

6011365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317541-A-G

6011393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317513-A-G

http://identifiers.org/hco/4/GRCh38#6011522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37317415-C-A

6011539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317397-C-T

6011779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37317255-A-G

6011885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37317171-G-A

6011885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37317171-G-C

http://identifiers.org/hco/4/GRCh38#6011961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#37317095-C-A

6011961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37317095-C-T

6011970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: splice acceptor variant
orthologous variants: 37317086-T-C

6014814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37313221-C-T

6014912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37313130-C-T

6017992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37312206-A-T

http://identifiers.org/hco/4/GRCh38#6018003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37312195-A-C

http://identifiers.org/hco/4/GRCh38#6018085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37312107-C-A

http://identifiers.org/hco/4/GRCh38#6018278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37311925-A-C

http://identifiers.org/hco/4/GRCh38#6018303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37311900-C-A

6018303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37311900-C-T

http://identifiers.org/hco/4/GRCh38#6018412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37311791-C-A

6018412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: missense variant
orthologous variants: 37311791-C-G

6018468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37311737-A-G

6018485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37311720-A-T

6018492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37311713-C-G

6018558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37311647-G-A

6018558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37311647-G-C

6018638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37311569-T-G

6018678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37311529-G-T

6018761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37311446-T-G

6019033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37311216-G-C

6019311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310964-A-G

6019448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310893-C-T

6019485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310837-G-T

6019965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37310510-T-C

6020035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310433-T-C

6020091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310390-A-G

6020168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310329-A-G

http://identifiers.org/hco/4/GRCh38#6020200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37310300-A-C

6020200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310300-A-G

http://identifiers.org/hco/4/GRCh38#6020209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37310280-C-A

http://identifiers.org/hco/4/GRCh38#6020210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37310279-C-A

6020306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310222-A-T

6020325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310205-C-G

6020426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310119-T-C

6020519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310019-G-A

6020519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37310019-G-T

http://identifiers.org/hco/4/GRCh38#6022140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37308977-C-A

6022216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37308909-C-T

6022233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37308884-G-C

6022791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308505-C-T

6022813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308483-G-A

6022882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308414-C-G

6022882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308414-C-T

6022887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308409-A-G

6023021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308266-G-C

6023021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308266-G-T

6023241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308017-C-T

6023242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37308016-G-A

6023596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37307682-C-T

6023735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37307578-C-T

6023736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37307562-C-T

6023766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37307532-C-T

6024542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37306876-G-C

6024558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37306861-G-A

6024612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37306811-A-G

6024642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5 prime UTR variant
orthologous variants: 37306782-C-T

6025042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37306413-A-T

6025269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37306227-C-T

6025364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37306142-A-G

6025517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37306017-T-A

6025738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37305789-T-A

6025947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37305627-C-T

6026131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37305439-T-A

6026142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37305431-G-A

6026142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37305431-G-C

6026142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37305431-G-T

6026553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304965-C-T

6026600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304937-G-A

http://identifiers.org/hco/4/GRCh38#6026629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37304912-C-A

6026668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304877-G-A

6026672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304873-C-T

6027059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304760-T-A

6027059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304760-T-C

6027353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304485-C-T

6027442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304401-A-G

http://identifiers.org/hco/4/GRCh38#6027542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37304321-C-A

6027542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304321-C-T

6027610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304268-G-A

6027690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37304186-C-G

6029801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37300115-G-A

6029801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37300115-G-T

6029852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37300086-A-G

6029893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37300047-T-C

6029894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37300046-G-A

6029894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37300046-G-T

6035388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299678-C-G

6035496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299592-G-A

6035745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299331-G-C

http://identifiers.org/hco/4/GRCh38#6035767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37299304-C-A

6035767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299304-C-T

6035804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299267-A-T

http://identifiers.org/hco/4/GRCh38#6035810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37299262-C-A

6035810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299262-C-G

6035810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299262-C-T

http://identifiers.org/hco/4/GRCh38#6035827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37299246-C-A

6035827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299246-C-G

http://identifiers.org/hco/4/GRCh38#6035847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37299219-C-A

6035847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299219-C-T

http://identifiers.org/hco/4/GRCh38#6035851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37299215-C-A

6035851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299215-C-G

6035851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299215-C-T

http://identifiers.org/hco/4/GRCh38#6035859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37299199-C-A

6035859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299199-C-T

6035877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299178-G-A

6035880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299175-G-T

6035891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37299167-T-C

6035973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 37299089-G-A

6035973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 37299089-G-T

6036100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 37298962-T-A

6036100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 37298962-T-C

6036183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37298888-T-A

6036183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37298888-T-C

6036183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37298888-T-G

6036190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37298881-A-G

6036217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37298869-G-A

6036217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37298869-G-T

6036399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37298721-A-G

http://identifiers.org/hco/4/GRCh38#6036468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37298671-C-A

6038901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37295598-C-T

http://identifiers.org/hco/4/GRCh38#6039019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37295480-C-A

6039214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37295314-G-A

6040784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37292832-G-A

6040784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37292832-G-T

6040813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37292813-T-C

6040813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37292813-T-G

6040875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37292766-C-G

6041547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37292074-G-A

6041729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291938-T-C

6041755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291918-G-A

6041766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291907-C-T

6041811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291867-C-G

6041971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291785-A-T

6041982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291775-A-G

http://identifiers.org/hco/4/GRCh38#6042057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37291722-C-A

6042057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291722-C-T

6042070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291711-A-G

6042070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291711-A-T

6042085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291700-A-G

6042090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291695-T-C

6042090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291695-T-G

6042092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291694-C-T

http://identifiers.org/hco/4/GRCh38#6042105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37291681-C-A

6042105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291681-C-T

http://identifiers.org/hco/4/GRCh38#6042135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37291670-C-A

6042135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291670-C-T

6042136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291669-C-G

6042136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291669-C-T

http://identifiers.org/hco/4/GRCh38#6042277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37291532-C-A

6042277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291532-C-G

6042277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291532-C-T

6042280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291529-A-G

http://identifiers.org/hco/4/GRCh38#6042296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37291516-C-A

6042327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291495-C-T

http://identifiers.org/hco/4/GRCh38#6042368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37291469-A-C

6042368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291469-A-T

6042490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291372-G-A

6042495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291367-T-A

6042623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291315-G-C

6042629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291309-G-A

http://identifiers.org/hco/4/GRCh38#6042718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37291222-A-C

6042743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291197-C-T

6042967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291022-G-C

6042972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291017-G-A

6042981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37291008-C-T

6043070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290983-T-C

6043251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290853-G-T

6043376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290781-G-A

6043386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290776-C-T

6043430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290734-C-G

6043435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290729-C-T

6043447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290717-C-T

6043485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290679-T-C

6043630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290560-G-C

http://identifiers.org/hco/4/GRCh38#6043692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37290505-A-C

http://identifiers.org/hco/4/GRCh38#6043928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37290271-C-A

6044106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290053-G-T

6044191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37290005-G-A

6044217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289981-C-T

6044252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289953-T-C

6044370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289823-G-C

6044462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289776-G-A

6044859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289342-G-C

6044869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289330-G-A

6044869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289330-G-C

http://identifiers.org/hco/4/GRCh38#6044992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37289209-C-A

6044998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37289203-G-C

6045018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289184-G-C

6045081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37289121-A-G

http://identifiers.org/hco/4/GRCh38#6045082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37289120-C-A

http://identifiers.org/hco/4/GRCh38#6045247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37288939-C-A

6045247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288939-C-T

6045320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288855-A-G

6045344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288831-T-C

6045438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288743-T-C

6045503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288681-A-T

6045926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288552-A-G

6045979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288500-G-A

6046233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288297-A-G

6046238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288292-G-A

6046250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288280-G-T

6046315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288230-C-T

6046320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288225-T-A

6046320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288225-T-C

6046349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288196-G-A

http://identifiers.org/hco/4/GRCh38#6046493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37288068-C-A

6046493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288068-C-T

6046496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288065-C-T

http://identifiers.org/hco/4/GRCh38#6046524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37288038-C-A

6046556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288004-A-G

6046556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37288004-A-T

6046616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287952-T-G

6046664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287904-T-C

6046674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287895-C-T

6046772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287816-A-G

6046843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287789-C-T

6046854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287772-T-C

6046887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287742-C-T

6047101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287629-C-G

6047187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287594-A-G

6047203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287578-G-A

http://identifiers.org/hco/4/GRCh38#6047221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37287563-C-A

6047221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287563-C-T

6047428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287371-G-C

6047511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287298-G-A

6047582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37287228-C-G

6047862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286958-G-A

6048022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286778-A-G

6048180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286615-G-A

6048355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286490-T-G

6048359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286486-T-C

6048663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286188-G-A

6048728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286125-G-A

6048728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286125-G-C

6048728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286125-G-T

http://identifiers.org/hco/4/GRCh38#6048765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37286088-C-A

6048808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286045-C-T

6048816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286038-C-G

6048816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: 37286038-C-T

http://identifiers.org/hco/4/GRCh38#6048970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37285886-C-A

http://identifiers.org/hco/4/GRCh38#6049418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37285794-C-A

http://identifiers.org/hco/4/GRCh38#6049669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37285538-C-A

6049669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285538-C-G

6049669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285538-C-T

http://identifiers.org/hco/4/GRCh38#6049675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37285532-C-A

6049675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285532-C-T

6049676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285531-A-T

http://identifiers.org/hco/4/GRCh38#6049685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37285522-C-A

6049685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285522-C-G

6049685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285522-C-T

6049740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285463-A-G

6049915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285304-G-A

6049915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285304-G-T

http://identifiers.org/hco/4/GRCh38#6049940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37285280-C-A

6049940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285280-C-T

6049943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285277-G-A

http://identifiers.org/hco/4/GRCh38#6049966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37285273-C-A

6049966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285273-C-T

6050017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 37285222-G-C

6050017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 37285222-G-T

6050080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285160-C-T

6050096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285147-C-T

6050319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37285022-G-A

http://identifiers.org/hco/4/GRCh38#6050461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37284938-C-A

6050468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284931-G-A

6050468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284931-G-C

6050532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284873-G-A

6050532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284873-G-T

6050656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 37284742-T-A

http://identifiers.org/hco/4/GRCh38#6050810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37284615-C-A

6050810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284615-C-T

6050836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284592-C-T

6050929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284519-G-A

6050989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284462-A-T

6051033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37284420-A-G

http://identifiers.org/hco/4/GRCh38#6051888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37283956-C-A

6052080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37283829-G-A

6052128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37283786-T-G

6053189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37283164-C-T

6053369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37282999-G-A

6053398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: intron_variant, undefined
orthologous variants: 37282977-A-G

6053894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37282504-G-C

6053894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37282504-G-T

6054227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37282126-G-T

http://identifiers.org/hco/4/GRCh38#6054240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37282113-C-A

6054240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37282113-C-G

http://identifiers.org/hco/4/GRCh38#6054247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37282106-C-A

6054247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37282106-C-T

http://identifiers.org/hco/4/GRCh38#6054254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37282099-C-A

6054254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37282099-C-T

6054422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281972-T-C

6054465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281930-T-A

6054607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281779-G-A

6054817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281615-T-G

6054850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281582-A-G

6054854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281578-T-A

6054904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281538-G-A

6054904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281538-G-T

6054994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281468-G-T

6055129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281344-G-A

6055402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37281067-A-G

6055598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37280916-C-G

6055598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37280916-C-T

6056630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37280721-T-C

6056641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37280715-C-T

6056659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37280708-C-T

6056773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37280607-C-T

6056886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37280546-T-A

6057322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37280145-G-A

6057431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37279976-T-C

6057557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37279836-C-G

6057557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37279836-C-T

http://identifiers.org/hco/4/GRCh38#6057583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37279818-C-A

6057613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37279788-T-A

6057621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37279780-C-G

6057621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37279780-C-T

6057811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37279597-A-G

6057847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37279551-G-A

6060102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37278678-G-A

6060139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37278635-A-T

6060319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37278473-T-C

http://identifiers.org/hco/4/GRCh38#6060321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37278471-C-A

6060321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37278471-C-T

http://identifiers.org/hco/4/GRCh38#6060324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37278462-C-A

6060324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37278462-C-T

http://identifiers.org/hco/4/GRCh38#6060372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37278417-C-A

6060372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37278417-C-T

http://identifiers.org/hco/4/GRCh38#6060986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37277840-A-C

6061203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37277445-T-G

6061485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37277100-T-C

6061495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37277090-C-T

6061538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37277053-C-T

6061572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37277041-C-T

6061721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276893-G-A

6061846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276785-C-T

6061985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276665-G-A

6061985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276665-G-T

http://identifiers.org/hco/4/GRCh38#6062013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37276632-C-A

6062102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276483-C-T

6062197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276396-C-G

6062197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276396-C-T

6062275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276288-G-A

6062303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276258-T-C

6062303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276258-T-G

6062499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276086-T-A

6062499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37276086-T-C

http://identifiers.org/hco/4/GRCh38#6062544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37276070-C-A

http://identifiers.org/hco/4/GRCh38#6062566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37276048-A-C

6062655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275960-G-A

6062709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275913-C-T

6063810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275492-G-A

6063850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275453-C-T

6063909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275399-G-A

http://identifiers.org/hco/4/GRCh38#6063914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37275394-C-A

6063914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275394-C-T

6063917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275391-G-A

6064120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275262-G-A

http://identifiers.org/hco/4/GRCh38#6064526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37275165-C-A

6064536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275154-C-G

6064536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37275154-C-T

http://identifiers.org/hco/4/GRCh38#6064573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37275123-A-C

http://identifiers.org/hco/4/GRCh38#6064748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37274995-C-A

http://identifiers.org/hco/4/GRCh38#6064765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37274980-C-A

6064765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274980-C-T

6064791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274971-G-T

6064826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274942-G-T

6064926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37274866-T-C

6065093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274717-G-A

6065093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274717-G-C

6065093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274717-G-T

6065124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274691-G-A

6065210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274595-C-T

http://identifiers.org/hco/4/GRCh38#6065473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37274408-A-C

6065742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274186-C-T

6065812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274113-T-C

6065923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37274006-C-T

6066020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273910-G-A

6066049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273883-A-G

6066088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273848-G-A

6066130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273807-A-G

http://identifiers.org/hco/4/GRCh38#6066156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37273787-A-C

6066247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273709-G-A

http://identifiers.org/hco/4/GRCh38#6067858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37273321-C-A

6067858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273321-C-G

6067887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273293-A-G

6068020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273109-G-A

6068032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37273097-T-C

6068243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272962-G-A

6068245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272960-T-A

6068349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272890-C-G

6068360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272879-T-A

6068411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272829-C-T

6068427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272813-T-C

6068470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272770-G-A

6068486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272757-C-T

6068508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272735-G-A

6068508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272735-G-C

6068597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272611-G-A

6068597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272611-G-C

6068597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272611-G-T

6068701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272519-G-A

6068765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272471-T-C

6068786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272453-T-G

6069014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272320-T-C

6069081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272258-A-G

6069164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272183-A-G

6069177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272171-C-T

6069389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37272027-A-G

6069636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271833-C-T

6069706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271738-T-C

http://identifiers.org/hco/4/GRCh38#6069942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37271337-C-A

6069942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271337-C-T

http://identifiers.org/hco/4/GRCh38#6069964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37271315-C-A

6069964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271315-C-T

6070014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271268-G-A

6070014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271268-G-T

http://identifiers.org/hco/4/GRCh38#6070049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37271239-C-A

6070104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37271184-A-G

6070109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 37271179-G-A

6070109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 37271179-G-T

6070168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271118-C-T

http://identifiers.org/hco/4/GRCh38#6070175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37271111-C-A

6070175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271111-C-T

6070177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271109-G-A

6070177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271109-G-T

6070189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37271099-G-A

6070448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37270917-G-A

6070458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37270905-G-T

6070475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37270883-G-C

6070529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37270831-A-G

6073962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37269055-G-C

6074036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37268974-T-A

6076276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37266358-G-A

6076295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37266339-C-T

6076394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37266271-T-G

6077092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37266021-T-A

6077330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37265779-A-G

6077383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37265730-G-C

6077484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37265628-T-C

6077896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37265371-C-T

6077959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37265301-T-C

6078651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37264904-G-A

6078812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37264754-A-G

http://identifiers.org/hco/4/GRCh38#6078874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37264701-C-A

6078874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37264701-C-T

6079007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37264592-A-G

6079033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37264562-A-G

6079375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37263747-G-A

http://identifiers.org/hco/4/GRCh38#6079578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37263577-C-A

6079698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37263474-A-G

6080029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37263195-G-A

6080029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37263195-G-T

6080033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37263191-G-A

6080033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37263191-G-T

6080053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37263175-C-T

6080058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37263170-T-C

6080290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 37262975-G-A

6080364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262911-G-A

6080364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262911-G-C

6080393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262882-G-T

6080396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262879-T-C

6080399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262876-A-G

6080406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262868-G-T

6080945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262736-G-A

6080981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262707-A-T

6080984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262704-T-C

6081187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262585-G-A

6081364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262447-G-A

6081364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262447-G-C

6081567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262314-G-A

6081661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 37262249-A-G

http://identifiers.org/hco/4/GRCh38#6081773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37262138-C-A

6081810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262100-G-A

6081810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37262100-G-C

6083462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37260830-T-C

http://identifiers.org/hco/4/GRCh38#6083488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37260800-A-C

6083488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37260800-A-T

6083610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37260684-A-G

6083861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37260148-T-G

6084425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37259614-T-C

6084642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37259444-A-G

6084712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37259332-G-A

6084712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37259332-G-T

6084714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37259330-A-G

http://identifiers.org/hco/4/GRCh38#6084719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37259325-A-C

6084719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37259325-A-G

6085046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37259051-T-A

6085132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37258963-T-A

6085132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37258963-T-C

6085394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37258213-G-A

http://identifiers.org/hco/4/GRCh38#6085402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37258205-C-A

6085402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37258205-C-T

6085638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37257969-G-A

6085638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37257969-G-C

6085638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37257969-G-T

6085672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37257934-G-A

6085672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37257934-G-T

6085741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37257889-G-C

6085741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37257889-G-T

6086384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37257585-C-T

http://identifiers.org/hco/4/GRCh38#6086715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37257234-C-A

6089883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37256473-A-G

6104126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37250297-T-G

6104600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249924-T-C

6104633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249892-T-C

6104674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249853-G-A

6104674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249853-G-T

6104779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249747-C-T

6105074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249402-G-A

6105082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249390-T-G

6105130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249327-C-G

6105130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249327-C-T

6105246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249202-G-A

6105352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249054-G-T

6105407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37249014-A-T

6105480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37248956-C-T

6105537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37248899-T-G

6105555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37248881-G-A

6105555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37248881-G-T

6105810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37248626-T-C

6105897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37248539-G-A

6105897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37248539-G-T

6105927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37248509-T-C

6105962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 37248474-G-T

6105993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37248452-G-A

6105993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37248452-G-T

6106006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37248439-G-A

6106006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37248439-G-T

6106007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37248438-T-A

6109704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37245410-C-T

6109938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37245176-A-G

6111493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37243387-G-A

6112465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37243051-C-G

6112522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242994-T-C

6112559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242949-G-A

6112574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242934-C-T

http://identifiers.org/hco/4/GRCh38#6112717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37242845-C-A

6112819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37242743-T-C

6112916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242656-G-A

6112964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242608-T-G

http://identifiers.org/hco/4/GRCh38#6113080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37242504-A-C

6113080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242504-A-G

http://identifiers.org/hco/4/GRCh38#6113097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37242487-C-A

6113097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242487-C-T

http://identifiers.org/hco/4/GRCh38#6113113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37242471-C-A

6113113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242471-C-T

http://identifiers.org/hco/4/GRCh38#6113129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37242455-C-A

6113164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242422-G-A

http://identifiers.org/hco/4/GRCh38#6113322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37242306-C-A

6113409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242235-A-T

6113428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242218-A-G

6113428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242218-A-T

6113611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37242009-A-G

6133166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37238030-G-A

6133465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237689-G-C

6133523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237654-T-A

6133551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237626-T-C

6133568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237609-C-T

6133573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237604-T-C

6133595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237582-G-A

6133595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237582-G-C

6133760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237438-T-C

6133761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237437-G-A

6133795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237406-T-A

6133920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237272-A-G

6133936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237256-C-T

6133971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37237213-G-C

6148222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37235300-G-A

6148222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37235300-G-T

6148417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37235107-G-A

6148465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37235051-G-A

6148613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37234891-T-C

6148636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37234868-G-A

6148641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37234860-G-C

6150378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37225540-G-A

6150449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37225468-T-C

6150458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37225459-A-G

http://identifiers.org/hco/4/GRCh38#6150479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37225443-C-A

6150535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37225388-G-T

6150608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37225349-G-A

6150654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37225334-C-G

6150654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37225334-C-T

6150909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37225080-C-T

6151009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37224919-A-G

6151209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37224744-T-C

6151498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37224561-C-T

6151557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37224511-G-A

6151731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37224351-G-A

6151755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37224330-T-G

6151812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37224281-C-G

http://identifiers.org/hco/4/GRCh38#6151888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37224209-A-C

6153871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37222739-C-T

6153960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37222690-C-T

6153996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37222661-T-A

6154392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37222302-G-T

6154831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221924-C-T

6154840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221915-C-G

6154864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221891-A-G

6154925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221847-G-A

6154945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221829-G-A

6155093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221693-T-C

6155100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221686-A-G

6155100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221686-A-T

6155109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221677-G-T

6155368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37221441-A-G

6156379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37219512-G-A

6156485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37219420-G-T

6156566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37219344-G-A

6156591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37219319-C-T

6156595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37219315-T-A

6156595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37219315-T-C

http://identifiers.org/hco/4/GRCh38#6156650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37219258-A-C

6156944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37219011-G-A

6156946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37219009-C-T

6157649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37218853-C-T

6176191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37207436-G-T

6176302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37207351-T-C

http://identifiers.org/hco/4/GRCh38#6176419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37207255-C-A

6176447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37207213-T-C

6176548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37207115-T-C

6177316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37206163-G-C

6177332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37206145-A-G

6177413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37206055-A-G

http://identifiers.org/hco/4/GRCh38#6177440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37206048-A-C

6177657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37205857-G-A

6177657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37205857-G-C

6177767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37205772-C-T

6177835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37205710-G-C

6177985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37205570-G-A

6178067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37205510-G-A

6178067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37205510-G-C

6178067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37205510-G-T

6179256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37204892-C-G

6179303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37204849-T-C

http://identifiers.org/hco/4/GRCh38#6179304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37204848-A-C

http://identifiers.org/hco/4/GRCh38#6179450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37204714-C-A

6179450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37204714-C-T

6179503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37204646-G-A

6179762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37204424-C-T

6180138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37204110-T-A

6180500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37203714-G-A

6180934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37202547-T-A

6180958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37202524-G-C

6181037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37202447-C-T

6181491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37201989-T-A

6181575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37201894-G-A

http://identifiers.org/hco/4/GRCh38#6182608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37201239-C-A

6182608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 37201239-C-T

6182804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37201065-A-G

6182859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37201010-C-T

6182865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37201004-A-G

6183097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37200839-G-A

6183114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37200817-C-T

6184147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37199925-T-A

6184147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37199925-T-C

6184206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37199869-T-C

6184228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37199847-A-G

6184350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37199752-C-T

6184555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37199556-G-C

http://identifiers.org/hco/4/GRCh38#6187446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37197467-A-C

6187635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37197303-A-G

6187650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37197288-C-T

6187651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37197287-G-A

6187654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37197284-A-G

6187885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37197055-T-G

6188102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37196641-C-T

6188203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37196532-C-T

6193484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37193503-A-T

6193635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37193351-C-T

6193650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37193336-T-A

6193679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37193307-G-A

6193737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37193267-G-A

6193737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37193267-G-C

http://identifiers.org/hco/4/GRCh38#6194327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37193146-A-C

6194382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37193087-T-C

6194439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37193036-G-T

http://identifiers.org/hco/4/GRCh38#6194459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37193021-C-A

http://identifiers.org/hco/4/GRCh38#6194520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37192982-C-A

6194522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37192980-T-C

6194591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37192928-G-T

http://identifiers.org/hco/4/GRCh38#6194599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37192916-C-A

http://identifiers.org/hco/4/GRCh38#6194619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37192896-C-A

6194619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37192896-C-T

6194637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37192880-A-G

6194718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37192809-A-G

6194960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37192576-A-G

6194997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37192553-G-A

6195130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189928-C-T

6195132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189926-G-A

6195335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189782-G-A

6195685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189496-T-C

6195755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189444-G-A

6195755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189444-G-C

http://identifiers.org/hco/4/GRCh38#6195832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37189412-C-A

6196033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189219-T-C

6196112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189142-A-G

6196113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37189141-C-T

6196278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37188862-G-A

http://identifiers.org/hco/4/GRCh38#6196367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37188723-C-A

6196425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37188657-T-C

http://identifiers.org/hco/4/GRCh38#6196456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37188633-C-A

6196536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37188566-G-A

6198318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37187570-G-C

6198341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37187562-G-T

http://identifiers.org/hco/4/GRCh38#6198517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37187393-C-A

6198659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37187262-A-G

http://identifiers.org/hco/4/GRCh38#6198879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37187099-C-A

6198903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37187078-G-A

6198979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37187032-C-T

6199071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186950-A-G

http://identifiers.org/hco/4/GRCh38#6199077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37186944-A-C

6199077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186944-A-T

6199138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186876-A-T

6199176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186841-G-T

6199304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186760-T-C

http://identifiers.org/hco/4/GRCh38#6199377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37186712-C-A

6199619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186467-T-C

6199619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186467-T-G

6199651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186435-G-C

http://identifiers.org/hco/4/GRCh38#6199718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37186369-C-A

6199718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186369-C-T

6199946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186185-G-C

6200039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186104-G-A

6200103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186059-G-A

6200103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186059-G-T

6200131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186041-G-A

6200131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186041-G-T

http://identifiers.org/hco/4/GRCh38#6200149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37186024-C-A

6200149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186024-C-T

6200174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37186000-G-T

http://identifiers.org/hco/4/GRCh38#6200253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37185941-C-A

6200285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 37185909-G-A

6200285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 37185909-G-T

6200477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 37185748-G-A

http://identifiers.org/hco/4/GRCh38#6200537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37185706-C-A

6200552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33766
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37185691-A-G