37812566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7867183-A-T

37812592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7867157-G-A

37812592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7867157-G-T

37813037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866760-T-A

37813037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866760-T-C

http://identifiers.org/hco/5/GRCh38#37813048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7866748-C-A

37813048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866748-C-T

37813208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866622-A-G

37813251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866598-T-C

37813286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866559-A-T

37813375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866440-T-C

37813519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866292-G-A

37813519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866292-G-T

37813542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866270-T-C

37813974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866189-A-G

http://identifiers.org/hco/5/GRCh38#37814077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7866090-C-A

37814077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866090-C-T

37814131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866050-G-A

37814131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7866050-G-T

http://identifiers.org/hco/5/GRCh38#37814249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7865908-A-C

37814366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 7865802-A-G

http://identifiers.org/hco/5/GRCh38#37814384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7865792-C-A

37814384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 7865792-C-T

37814399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 7865774-A-G

http://identifiers.org/hco/5/GRCh38#37814419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7865523-C-A

37814419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 7865523-C-G

37814566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7865382-C-G

http://identifiers.org/hco/5/GRCh38#37815038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7864913-C-A

37815038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7864913-C-T

http://identifiers.org/hco/5/GRCh38#37815208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7864733-C-A

37815230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7864709-G-A

37815230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7864709-G-T

http://identifiers.org/hco/5/GRCh38#37815237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7864702-C-A

37815237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7864702-C-G

37815237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7864702-C-T

37815925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7864037-G-A

37815925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7864037-G-C

37816031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7863931-G-A

37816206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863759-G-A

37816206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863759-G-T

37816373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863585-A-G

37816589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863377-T-C

37816644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863324-T-G

37816722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863262-G-C

37816958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863072-A-G

37817303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7862769-A-G

37817375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7862694-T-C

37817494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7862560-C-G

37817549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7862505-G-A

http://identifiers.org/hco/5/GRCh38#37817770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7862294-C-A

37817807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7862258-G-A

37818655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860996-T-A

37818655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860996-T-C

37818740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860926-G-C

37818869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860868-A-T

37819040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860712-G-A

37819040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860712-G-T

37819143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860522-C-G

37819143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860522-C-T

37820096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859911-G-A

37820180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859826-G-A

37820180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859826-G-C

37821274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7856191-G-A

37821364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7856101-A-G

37821375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7856090-T-A

37821499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7855910-C-T

37821706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7855705-C-T

37821762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7855652-G-C

37822302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7855152-G-A

37822583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854938-C-T

37822587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854935-C-T

37822690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854849-G-T

37822832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854741-A-T

37822833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854740-A-G

37822890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854706-T-G

37823021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854588-T-C

http://identifiers.org/hco/5/GRCh38#37823212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7854193-C-A

37823212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854193-C-G

37823331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7854089-G-C

37823400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7854035-A-G

http://identifiers.org/hco/5/GRCh38#37823806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7853637-C-A

37823806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7853637-C-T

http://identifiers.org/hco/5/GRCh38#37823928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7853543-C-A

37823928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7853543-C-T

37824039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7853422-A-G

http://identifiers.org/hco/5/GRCh38#37824068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7853396-C-A

37824121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7853346-G-T

http://identifiers.org/hco/5/GRCh38#37824270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7853221-C-A

http://identifiers.org/hco/5/GRCh38#37824310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7853192-C-A

37824448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7853053-C-G

37824552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852971-C-G

http://identifiers.org/hco/5/GRCh38#37824554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7852969-C-A

37824656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852864-C-T

37824660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852860-G-T

37824693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852775-T-A

37824787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852699-C-T

37824942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852562-A-G

37825070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852433-C-T

37825083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852420-A-G

37825263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852252-T-C

37825274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852240-C-T

37826013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7851169-C-T

37826087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7851104-T-C

http://identifiers.org/hco/5/GRCh38#37826395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7850872-C-A

37826395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850872-C-T

37826477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850793-C-G

37826541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850672-G-A

37827203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850220-G-A

37827249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850190-A-T

37827544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849897-G-T

37828778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849562-A-T

37828889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849465-G-T

37829088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849298-A-G

37829178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849216-T-C

37829322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849106-T-C

37829337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849091-T-C

37829341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849086-A-G

37829447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849003-A-G

37829456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7848994-G-T

37829748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7848733-G-A

http://identifiers.org/hco/5/GRCh38#37829749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7848732-C-A

37831165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7848383-C-T

37831177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7848369-T-C

37831431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7848147-T-A

37831431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7848147-T-C

37831654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7847934-C-T

37831741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7847856-T-A

37831741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7847856-T-C

37832045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7847616-A-G

http://identifiers.org/hco/5/GRCh38#37832169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7847489-A-C

37832258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7847400-T-C

37832679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846989-C-T

37832877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846792-C-T

37832920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846750-A-G

37832985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846682-G-A

37832985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846682-G-C

37832985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846682-G-T

37832999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846667-T-C

37833276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846428-G-C

37833471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846261-A-G

37833649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846093-A-G

37833664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846078-T-G

37833675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846066-G-T

37834507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845375-C-T

37834540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845350-G-A

37834540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845350-G-T

37834603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845286-G-A

37834603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845286-G-C

37834609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7845280-G-A

37834609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7845280-G-C

37834609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7845280-G-T

37834810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7845080-C-T

37834831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7845059-G-A

37834831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7845059-G-T

http://identifiers.org/hco/5/GRCh38#37834906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844954-C-A

37834906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844954-C-G

37834906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844954-C-T

http://identifiers.org/hco/5/GRCh38#37834910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844950-C-A

37834910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844950-C-T

http://identifiers.org/hco/5/GRCh38#37834925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844927-C-A

http://identifiers.org/hco/5/GRCh38#37834928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844924-C-A

37834971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844882-T-C

http://identifiers.org/hco/5/GRCh38#37835051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844798-C-A

37835051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844798-C-T

37835220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844640-C-T

37835237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844614-C-T

37835271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844577-A-G

37835271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844577-A-T

http://identifiers.org/hco/5/GRCh38#37835281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844565-C-A

37835281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844565-C-G

37835281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844565-C-T

37835283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844563-G-A

37835283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844563-G-T

http://identifiers.org/hco/5/GRCh38#37835306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844537-C-A

37835306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844537-C-G

37835466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844371-G-A

37835466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844371-G-T

37835481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844357-T-C

37835481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844357-T-G

37835486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844352-T-A

37835486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844352-T-C

37835486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844352-T-G

37835499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844339-T-C

http://identifiers.org/hco/5/GRCh38#37835514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844324-A-C

http://identifiers.org/hco/5/GRCh38#37835580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844265-C-A

37835580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844265-C-T

37835622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844239-T-C

http://identifiers.org/hco/5/GRCh38#37835657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844204-A-C

37835657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844204-A-G

37835681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844180-C-T

37835699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844164-C-T

37835713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844150-G-T

37835721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7844142-C-T

http://identifiers.org/hco/5/GRCh38#37835906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7844031-C-A

37835906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7844031-C-G

37835942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843995-G-C

37835942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843995-G-T

http://identifiers.org/hco/5/GRCh38#37835951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7843983-C-A

37835951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843983-C-G

37835951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843983-C-T

37836012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843916-G-C

37836071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843857-C-T

37836179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843786-G-C

37836179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843786-G-T

37836378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843565-G-T

37836541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7843409-G-C

http://identifiers.org/hco/5/GRCh38#37836591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7843378-C-A

37836982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7842970-G-T

37837048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7842905-C-T

http://identifiers.org/hco/5/GRCh38#37837260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7842706-C-A

37837472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7842512-G-A

37837615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7842381-G-A

37838103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7841941-T-C

http://identifiers.org/hco/5/GRCh38#37838113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7841931-C-A

37838468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7841570-G-C

37838477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7841561-T-C

37838697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7841346-A-T

http://identifiers.org/hco/5/GRCh38#37838925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7841087-C-A

37839141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7840890-G-A

37839146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7840885-G-A

37839282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840755-G-A

http://identifiers.org/hco/5/GRCh38#37839391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7840683-C-A

37839471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7840630-C-G

37839471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7840630-C-T

37839580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840520-T-C

37839580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840520-T-G

37839632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840468-G-T

http://identifiers.org/hco/5/GRCh38#37839706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7840388-C-A

37839720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840374-G-A

37839720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840374-G-T

37839826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840265-T-C

http://identifiers.org/hco/5/GRCh38#37839841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7840250-C-A

37839841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840250-C-T

http://identifiers.org/hco/5/GRCh38#37839918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7840172-C-A

37839918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840172-C-T

37839962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840137-G-A

37839962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7840137-G-T

http://identifiers.org/hco/5/GRCh38#37840163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7839936-C-A

37840163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7839936-C-G

37840163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7839936-C-T

http://identifiers.org/hco/5/GRCh38#37840184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7839914-C-A

37840184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7839914-C-T

http://identifiers.org/hco/5/GRCh38#37840443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7839703-C-A

37840523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7839622-A-G

37840523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7839622-A-T

37840947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7839191-G-A

37841105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7839033-C-T

37841310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7838834-T-A

37841310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7838834-T-C

37841381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7838763-T-C

37841416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7838728-G-A

37841632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7838514-T-C

http://identifiers.org/hco/5/GRCh38#37841834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7838297-C-A

37841940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7838168-T-C

37842178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7837970-C-G

37842522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7837626-C-G

37842546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7837603-A-G

37843381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7836609-T-C

37843653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7836357-C-T

37843749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7836272-T-C

37843876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7836159-T-A

37844441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7835743-C-T

37844442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7835742-A-G

37844512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7835681-A-G

37844694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7835498-T-C

http://identifiers.org/hco/5/GRCh38#37845123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7835369-C-A

37845212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7835274-C-T

37845263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7835225-A-G

37845273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7835215-G-T

37845298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7835143-C-T

37846914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7832945-C-T

http://identifiers.org/hco/5/GRCh38#37846931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7832928-A-C

37846931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7832928-A-G

37846976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7832883-A-T

37847248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7830547-A-G

37847524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7830139-A-G

37847850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7829806-C-G

37847850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7829806-C-T

37847978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7829634-G-A

37848082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7829531-C-T

37848304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7829328-G-C

37848304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7829328-G-T

37848593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7829055-C-T

37848661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7828985-C-T

37848664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7828982-C-T

37849016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7828618-T-C

37849016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7828618-T-G

37850133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7827176-T-C

http://identifiers.org/hco/5/GRCh38#37850955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7826270-A-C

37850962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7826263-A-G

37850999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7826244-A-G

37850999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7826244-A-T

37851222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7826076-G-A

37851222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7826076-G-C

37851222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7826076-G-T

37851223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7826075-T-G

37851555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7825747-T-G

37851976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7825260-A-G

37852027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7825207-A-G

37852179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7825108-A-G

37852246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7825046-T-A

37852521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7824773-C-T

37852594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7824696-C-T

37852660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7824180-A-G

37852766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7824061-A-G

37853198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7823662-G-A

37853320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7823548-A-G

37853696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7823067-C-T

37853839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7822938-C-G

37854635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7822214-C-T

37854733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7822134-T-C

37854871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7822021-G-A

37854911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7821981-T-C

37857630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7819897-A-G

37857687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7819842-T-C

http://identifiers.org/hco/5/GRCh38#37858023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7819544-A-C

37858023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7819544-A-G

37859369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7817043-G-T

http://identifiers.org/hco/5/GRCh38#37859523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7816951-A-C

37859574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816889-C-T

37859615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816844-T-C

37859625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816834-G-C

37859668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816791-A-G

37859671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816788-G-C

37859779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816665-G-A

37859789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816646-G-A

37860026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816442-A-G

37860109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7816377-G-A

http://identifiers.org/hco/5/GRCh38#37860753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7815800-C-A

37861038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7815538-G-A

37861095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7815484-C-T

37863685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7813110-C-T

37863848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812974-T-A

37863890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812933-G-A

37863986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812848-T-C

37864043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812795-G-A

http://identifiers.org/hco/5/GRCh38#37864063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7812774-A-C

37864063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812774-A-G

37864078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812757-C-T

37864235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812603-C-G

37864235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812603-C-T

37864460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7812368-A-G

37864710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7811449-A-G

37864915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7811257-G-T

http://identifiers.org/hco/5/GRCh38#37865001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7811176-C-A

37865015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7811162-G-T

http://identifiers.org/hco/5/GRCh38#37865050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7811126-C-A

37865050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7811126-C-G

37865050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7811126-C-T

37865072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7811105-G-A

37865072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7811105-G-T

37865142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7811035-T-C

37865233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7810960-C-T

37865259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7810935-G-T

37865441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7808323-T-C

http://identifiers.org/hco/5/GRCh38#37865477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7808287-C-A

37865480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7808284-T-C

37865587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7808183-A-G

37865887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7807937-T-C

37866005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7807824-C-G

37866069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7807759-G-C

37866080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7807748-A-G

37866082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7807746-A-G

37866314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7807158-A-G

37866412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7807066-G-A

37866437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7807041-C-T

37866671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7806845-G-A

37866734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7806793-C-T

37866744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7806783-T-G

37869659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7805606-A-T

37869793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7805509-G-T

http://identifiers.org/hco/5/GRCh38#37869834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7805471-C-A

37869852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7805456-A-G

37869905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7805413-T-C

37869936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7805383-T-C

37870380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804613-A-G

37870426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804531-G-T

37870494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804468-G-T

http://identifiers.org/hco/5/GRCh38#37870563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7804408-C-A

37870577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804394-G-A

37870577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804394-G-C

37870577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804394-G-T

http://identifiers.org/hco/5/GRCh38#37870593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7804382-C-A

37870644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804333-C-T

37870786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804230-A-G

37870829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804183-T-C

37870888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804121-T-C

37870983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804065-A-G

37871052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7804006-G-A

37871406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803669-A-G

37871468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803607-T-C

37871547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803529-A-G

37871596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803485-T-C

37871729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803368-C-T

http://identifiers.org/hco/5/GRCh38#37871736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7803361-C-A

37871736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803361-C-T

37871743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803354-T-C

37871844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803255-T-C

37871872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803227-A-G

37871895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803204-T-C

37871990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7803109-G-T

37872168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7802930-G-A

37872484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7802614-T-C

37872593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7802504-G-T

37873337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7801547-C-T

37873510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7801363-T-C

37873518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7801355-G-T

http://identifiers.org/hco/5/GRCh38#37873543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7801323-C-A

37873646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7801217-T-C

37873666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7801158-A-G

http://identifiers.org/hco/5/GRCh38#37873830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7800998-A-C

http://identifiers.org/hco/5/GRCh38#37873853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7800983-C-A

http://identifiers.org/hco/5/GRCh38#37873889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7800973-C-A

37873892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7800970-G-A

37873892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7800970-G-T

37873912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7800957-C-T

http://identifiers.org/hco/5/GRCh38#37873971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7800901-C-A

37874057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7800845-G-T

http://identifiers.org/hco/5/GRCh38#37874248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7800723-A-C

37874289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7800681-T-C

37874315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7800663-T-C

37874351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7800622-T-A

37874367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7800606-T-C

37875137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798768-G-A

37875137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798768-G-T

37875168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 7798737-T-C

37875172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 7798733-G-A

37875172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 7798733-G-T

37875232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798676-T-C

37875286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798645-G-T

http://identifiers.org/hco/5/GRCh38#37875288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7798643-C-A

37875302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798642-A-G

37875321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798621-T-C

37875321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798621-T-G

37875341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798598-G-A

37875341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798598-G-T

37875494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798458-G-T

37875641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798350-G-C

37875641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798350-G-T

37875672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798334-T-C

37875689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798317-T-A

37875741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798274-G-T

37875769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 7798249-G-A

http://identifiers.org/hco/5/GRCh38#37875794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7798225-A-C

37875795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43592
most severe consequence: non coding transcript exon variant
orthologous variants: 7798224-T-G