3606794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654697-G-A

3606794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654697-G-T

http://identifiers.org/hco/12/GRCh38#3606999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127654505-A-C

3606999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654505-A-G

3607026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654480-G-A

3607139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654368-T-G

3607221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654303-A-G

3607412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654179-G-T

3607585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654012-A-G

3607585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127654012-A-T

3607642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127653955-T-C

http://identifiers.org/hco/12/GRCh38#3607754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127653847-C-A

3607754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127653847-C-T

3607778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127653823-A-G

3607959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127653671-A-G

3607992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127653633-G-A

3608566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127653053-T-A

3608710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127652918-G-A

http://identifiers.org/hco/12/GRCh38#3608737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127652902-A-C

3608770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127652868-T-C

3608830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127652845-G-C

3609064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127652649-T-C

3609270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127652451-A-G

3609334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127652218-A-G

3609640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127651871-C-T

3609697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127651814-C-G

3609697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127651814-C-T

3609759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127651739-A-G

http://identifiers.org/hco/12/GRCh38#3610192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127651337-C-A

3610226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127651302-T-G

3611295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127650017-G-T

3611468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127649835-G-T

3611474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127649829-T-C

3611839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127649549-G-T

3611846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127649543-A-G

3611847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127649542-G-C

3611847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127649542-G-T

3611967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127649423-G-T

3611976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127649413-A-G

3612009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127649380-G-T

3612103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127649289-T-C

3612206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127649181-G-A

3612206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127649181-G-C

3612206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127649181-G-T

3613214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127648274-G-A

3613215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127648273-G-A

3613238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127648147-G-A

3613339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127648051-C-T

3613410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127647985-C-T

3613491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127647903-A-G

3613638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127647759-C-T

3613824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127647531-C-T

3613918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127647439-T-C

3614003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127647382-G-A

3614295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127647117-T-A

3614599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127646813-G-C

3614897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127646563-G-A

3614897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127646563-G-T

http://identifiers.org/hco/12/GRCh38#3614911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127646549-C-A

http://identifiers.org/hco/12/GRCh38#3614912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127646548-C-A

3615097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127646363-G-A

3615097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127646363-G-T

3615248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 127646230-A-G

3615358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 127646085-G-A

3615460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127645968-G-A

3615464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127645964-C-T

http://identifiers.org/hco/12/GRCh38#3615486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127645942-C-A

3615486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127645942-C-T

http://identifiers.org/hco/12/GRCh38#3615664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127645816-C-A

3615729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127645753-C-T

3615836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127645682-C-G

3616268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127645375-G-A

http://identifiers.org/hco/12/GRCh38#3616315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127645328-A-C

3616315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127645328-A-G

http://identifiers.org/hco/12/GRCh38#3616405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127645277-A-C

3616981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127644596-G-A

3616986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 127644591-G-A

3617017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127644560-A-G

3617065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127644516-T-C

3617097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127644475-A-G

3617277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127644352-G-A

3617295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127644335-T-C

3617491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127644144-A-G

3617592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127644070-C-T

3617600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127644063-G-A

3617701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127643989-T-C

3617986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127643718-T-C

3618038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127643676-G-A

3618195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127643323-G-A

3618221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127643267-T-C

3618278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127643212-T-C

3618317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127643173-C-G

3618319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127643171-A-G

3618485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642982-A-T

3618689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642818-C-T

3618710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642797-A-G

3618718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642691-C-T

3618847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642530-T-A

3619047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642326-T-C

3619124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642263-T-C

3619130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642257-G-A

3619130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642257-G-T

3619197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642194-A-G

http://identifiers.org/hco/12/GRCh38#3619210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127642179-C-A

3619210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642179-C-T

3619213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642176-G-T

http://identifiers.org/hco/12/GRCh38#3619265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127642125-C-A

3619265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642125-C-G

3619265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642125-C-T

3619340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 127642050-C-T

3619391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127642000-T-C

3619523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127641902-G-T

3619524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127641901-A-T

3619679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127641787-G-A

3619775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127641657-C-T

3619779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127641648-G-A

3619819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127641617-G-A

3620603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127640841-A-G

3620878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127640600-T-A

3621091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127640383-G-A

3621185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127640288-G-C

3621204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127640269-C-T

3621308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127640159-T-G

3621946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127639858-C-T

3622520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127639197-G-A

3622526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127639191-C-T

3622874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127638822-G-T

3623006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127638692-G-A

http://identifiers.org/hco/12/GRCh38#3623741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127637990-C-A

3623741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127637990-C-T

3623805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127637900-G-A

3623805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127637900-G-C

3623805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127637900-G-T

3624070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127637112-A-G

http://identifiers.org/hco/12/GRCh38#3624087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127637094-A-C

3624179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127637001-T-C

3624426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127636749-C-G

3624614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127636563-T-C

3624705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127636498-T-G

3625024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127636283-T-A

3625024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127636283-T-C

3625063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127636242-T-C

3625284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127636050-C-G

3625575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127635764-T-A

3626033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127635231-T-C

3626037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127635226-T-A

3626070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127635193-G-A

3626082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127635181-C-T

3626208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127635055-C-T

3627380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127634933-A-G

3627498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127634823-T-C

3627498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127634823-T-G

3627580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127634744-G-A

3627580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127634744-G-C

3627620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127634691-C-T

3627736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127634575-G-A

3627736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127634575-G-T

http://identifiers.org/hco/12/GRCh38#3627818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127634504-C-A

3628379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127632789-G-A

3628398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127632770-G-A

3628528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127632643-G-A

3629007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127632057-C-T

3629088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127631993-C-G

3629088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127631993-C-T

3629663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127631402-G-T

3629842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127631222-A-G

3629881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127631187-A-G

3630000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127631068-G-A

3630060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127631021-G-A

3630299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127630824-G-A

3630534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127630586-G-A

3630534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127630586-G-T

3630891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127630075-G-A

3630988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127629979-G-T

3631461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127629116-C-T

3631509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127629069-G-A

3633232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127627456-G-C

http://identifiers.org/hco/12/GRCh38#3633653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127626889-C-A

3633653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 127626889-C-T

3633897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127626672-A-G

3634740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127624679-G-A

3635153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127624335-G-A

3636171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127622855-G-A

3636185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127622841-G-C

3636305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127622753-C-T

3636364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127622730-T-G

3638065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621777-A-G

http://identifiers.org/hco/12/GRCh38#3638143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127621725-C-A

3638157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 127621711-T-G

3638197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127621671-G-A

3638197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127621671-G-T

3638198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127621670-G-C

3638205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 127621663-T-C

3638318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 127621550-T-A

3638318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127621550-T-C

3638368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127621500-G-A

3638463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 127621402-G-A

3638488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621374-G-T

http://identifiers.org/hco/12/GRCh38#3638520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127621351-A-C

3638540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621338-G-C

3638540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621338-G-T

3638577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621310-T-A

3638580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621307-G-A

3638580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621307-G-C

3638580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621307-G-T

3638652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621209-G-A

3638847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127621041-G-A

3638889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127620999-G-A

3639226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127620622-T-C

3639245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127620605-C-G

3639245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127620605-C-T

3639286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127620561-A-G

3639664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127620097-G-A

3639676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127620082-C-G

3639947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619757-T-A

3639973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619731-T-A

3639981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619723-T-G

3640007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619683-G-C

3640046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619638-T-C

3640279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619403-T-G

3640317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619366-G-T

3640345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619341-G-A

3640345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127619341-G-T

3640417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127619269-A-G

http://identifiers.org/hco/12/GRCh38#3640479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127619232-C-A

3640673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 127619034-G-A

3640673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127619034-G-T

3640812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618894-G-A

3640812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618894-G-C

3640812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618894-G-T

3640844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618866-C-G

3640861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618847-G-T

3640866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618842-T-C

3640878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618829-A-G

3641487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618523-C-G

3641520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618492-G-A

3641547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618466-A-G

3641604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618409-G-T

3641644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618361-G-A

3641644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618361-G-T

3641665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618347-T-C

3641666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618346-G-A

3641666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618346-G-T

3641682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618330-C-T

3641696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618317-G-A

3641696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618317-G-C

3641696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618317-G-T

3641710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127618296-T-A

http://identifiers.org/hco/12/GRCh38#3641981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127618042-C-A

3641981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127618042-C-T

http://identifiers.org/hco/12/GRCh38#3642047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127617972-C-A

3642586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127617827-G-T

3642708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127617692-G-A

3642775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127617624-C-T

3642777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127617622-C-T

3642783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127617616-G-A

3642901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127617502-C-T

3642902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127617501-T-G

3643173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127617211-C-G

3643543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616794-C-T

3643609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616737-T-C

3644281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616482-G-A

3644288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616475-T-G

http://identifiers.org/hco/12/GRCh38#3644348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127616416-C-A

3644348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616416-C-T

3644470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616308-G-A

3644470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616308-G-T

3644524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616241-G-A

3644524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616241-G-C

3644554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616203-G-T

3644560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616197-G-A

3644560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616197-G-C

3644578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616187-G-A

3644578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616187-G-C

http://identifiers.org/hco/12/GRCh38#3644697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127616069-A-C

3644703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616063-G-T

http://identifiers.org/hco/12/GRCh38#3644714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127616052-A-C

3644714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127616052-A-G

3644798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615993-G-A

3644863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615932-C-T

3645024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615816-T-A

3645078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615767-C-T

http://identifiers.org/hco/12/GRCh38#3645173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127615676-A-C

3645196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615653-G-A

3645222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615630-T-C

3645369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615481-A-G

3645370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615480-G-C

3645393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615456-G-A

3645500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127615352-A-G

http://identifiers.org/hco/12/GRCh38#3647129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127614379-A-C

3647203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127614307-C-G

3647203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127614307-C-T

3647269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127614241-C-G

3647269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127614241-C-T

3647456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127614068-C-G

http://identifiers.org/hco/12/GRCh38#3647497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127614027-A-C

3647548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127613905-G-C

3647763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127613836-A-G

3648383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127613636-G-A

3648383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127613636-G-T

http://identifiers.org/hco/12/GRCh38#3648394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127613625-C-A

3648394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127613625-C-G

3648584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 127613523-T-C

3649774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127613406-G-C

3649827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127613353-G-A

3650020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127613139-T-C

http://identifiers.org/hco/12/GRCh38#3650118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127613047-C-A

3650118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127613047-C-T

3650119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127613046-G-A

3650238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127612954-T-C

3650242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127612950-C-T

3650275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127612926-G-C

3650348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127612846-T-C

3651122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127612082-A-T

3651147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127612057-T-A

3651923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127611189-A-G

3652462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127610740-G-A

3652462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127610740-G-T

3652482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127610720-T-A

3652566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127610638-G-A

http://identifiers.org/hco/12/GRCh38#3652616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127610577-A-C

3653969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127609301-G-T

3654070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127609075-G-A

3654070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127609075-G-T

3654074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127609071-G-C

3654074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127609071-G-T

3654082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127609063-T-C

3654232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 127608928-T-G

3654379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 127608781-G-A

http://identifiers.org/hco/12/GRCh38#3654418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127608746-C-A

http://identifiers.org/hco/12/GRCh38#3654467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127608707-C-A

3654467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127608707-C-G

3654467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127608707-C-T

3654475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127608699-G-A

3654475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127608699-G-T

3654543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127608672-T-C

http://identifiers.org/hco/12/GRCh38#3655062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127608136-C-A

3655205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127607995-T-A

3655270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127607930-G-T

3655276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127607924-T-A

3655617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127607609-G-A

3656223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606877-T-C

3656246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606860-G-A

3656246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606860-G-T

3656289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606817-G-T

3656443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606664-T-A

3656443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606664-T-C

3656448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606659-C-T

3656653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606461-T-A

3656663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606451-C-T

3656851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606304-G-A

3657039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127606090-G-A

3657611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127605568-C-T

3657631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127605547-C-T

3657872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127605318-A-G

3657954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127605236-C-T

3658193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604996-T-C

3658212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604977-G-A

3658212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604977-G-C

3658301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604909-G-A

3658379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604835-A-T

3658625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604595-G-A

3658648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604572-C-T

3658792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604434-A-G

http://identifiers.org/hco/12/GRCh38#3658838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127604398-A-C

3658838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604398-A-T

3658936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127604303-A-G

3659091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127603857-T-C

3659263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127603168-G-A

3659488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602976-A-G

http://identifiers.org/hco/12/GRCh38#3659496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127602966-A-C

3659496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602966-A-T

3659526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602925-G-A

3659526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602925-G-T

http://identifiers.org/hco/12/GRCh38#3659527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127602924-C-A

3659552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602898-G-A

3659583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 127602867-T-C

3659601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 127602849-T-C

3659637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127602813-T-A

3659637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127602813-T-C

3659637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 127602813-T-G

3659669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602784-A-T

3659685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602768-G-T

3659688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602765-G-T

3659751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602706-T-A

3659753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602704-G-A

3659753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602704-G-T

3659754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602703-G-A

3659754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602703-G-T

http://identifiers.org/hco/12/GRCh38#3659803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127602661-C-A

3659852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602611-C-G

3659852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602611-C-T

3659941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602536-C-T

3660021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602464-C-T

3660100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602389-T-C

3660121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602368-T-C

3660206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602293-C-T

3660207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127602292-A-G

3660849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127601725-C-T

3661060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127601540-T-C

3661183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127601427-A-G

3661238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127601368-T-A

3661512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127601109-A-G

3661816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127600844-A-G

3662174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127600496-T-C

3662264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127600420-C-T

3662432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127600266-C-T

3662442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127600256-C-G

3662442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127600256-C-T

3662479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127600216-A-T

3662527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127600168-A-G

3662886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127599834-A-G

3662908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127599812-A-G

3663143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127599536-T-C

3663263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127599403-C-T

3663601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127598906-C-T

3663698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127598819-T-G

3663726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127598791-C-T

3663918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127598620-A-G

3663918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127598620-A-T

3663959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127598581-T-G

3664145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127598413-T-C

http://identifiers.org/hco/12/GRCh38#3664177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127597998-A-C

3664290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597873-T-A

3664327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597836-G-A

3664394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597751-T-C

3664429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597718-A-G

3664470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597675-C-T

3664482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597664-G-A

3664520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597626-T-C

3664575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597419-G-A

3665095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597271-A-G

3665342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127597025-A-T

3666350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127596150-T-G

3666352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127596148-T-C

3666372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127596078-C-T

3666384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127596066-C-T

3666391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127596059-G-A

3666594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127595890-G-A

3666676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127595809-C-T

3666702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127595783-C-T

3667180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127595133-A-G

3667326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127595005-T-C

3667337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127594994-A-G

3668009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127594466-C-T

3668051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127594424-C-T

3668083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127594392-G-A

3668262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127594231-T-A

3668644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127593586-T-C

http://identifiers.org/hco/12/GRCh38#3668808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127593431-A-C

3668808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127593431-A-G

3668975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127593295-C-T

3669377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127592926-A-G

3669843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127591893-G-C

3669845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127591891-G-T

3670166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127591426-C-T

http://identifiers.org/hco/12/GRCh38#3670240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127591381-A-C

3670329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127591292-C-T

3670337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127591284-C-T

3670762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590720-G-A

http://identifiers.org/hco/12/GRCh38#3670838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127590642-C-A

3670877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590613-T-A

3670893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590605-T-A

3670893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590605-T-C

3670911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590589-G-A

3670990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590539-G-A

3671005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590524-A-G

3671157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590370-T-C

3671299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590240-C-T

3671382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590158-G-A

3671520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127590054-C-T

3671722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127589985-G-C

3671756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127589949-T-G

3671863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127589868-T-C

3671907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127589820-G-A

3672071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127589676-A-G

3672167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127589589-T-C

3672445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127589377-C-G

3672743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127589094-T-G

http://identifiers.org/hco/12/GRCh38#3672981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127588948-C-A

3673097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127588824-T-C

3673254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127588663-T-C

3673343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127588567-A-T

3673363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127588547-G-A

3673363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127588547-G-C

3673363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127588547-G-T

3673500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 127588439-G-A

3673500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 127588439-G-C

3673539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: stop gained
orthologous variants: 127588400-A-T

http://identifiers.org/hco/12/GRCh38#3673612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127588324-C-A

3673612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588324-C-T

http://identifiers.org/hco/12/GRCh38#3673639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127588298-A-C

3673639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588298-A-T

3673642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588295-G-A

3673672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588265-G-C

3673672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588265-G-T

3673675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588262-A-G

3673675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588262-A-T

3673686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588251-G-C

3673686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588251-G-T

3673688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588249-A-G

3673696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588241-A-G

http://identifiers.org/hco/12/GRCh38#3673713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127588229-C-A

3673728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588215-A-G

3673728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588215-A-T

3673734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588209-T-A

3673742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588201-G-A

3673742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588201-G-C

3673742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588201-G-T

3673852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588160-G-T

3673861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588151-G-C

3673920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127588099-T-A

3674109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127587938-G-A

3677065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127587010-A-G

3677137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127586954-G-A

3677137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127586954-G-C

http://identifiers.org/hco/12/GRCh38#3677588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127586572-C-A

3677744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127586457-C-T

3677812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127586382-G-A

3677828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127586360-G-C

3678600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585833-A-T

3679003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 127585619-C-T

3679109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585514-C-G

3679109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585514-C-T

3679161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585462-T-C

3679162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585461-C-T

3679180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585443-T-C

3679210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585417-A-G

3679212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585415-G-A

3679212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585415-G-T

http://identifiers.org/hco/12/GRCh38#3679221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127585406-C-A

3679221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585406-C-T

3679222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585405-T-C

3679222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585405-T-G

http://identifiers.org/hco/12/GRCh38#3679223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127585404-C-A

3679345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127585288-G-T

3679679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584805-T-C

3679691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584783-T-C

3679832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584646-A-G

3679849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584629-G-A

3679946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584535-T-C

3679969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584517-C-T

3680007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584491-G-A

3680018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584480-T-C

3680038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584461-C-T

http://identifiers.org/hco/12/GRCh38#3680091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127584408-C-A

3680091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584408-C-T

http://identifiers.org/hco/12/GRCh38#3680100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127584399-C-A

3680100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584399-C-G

3680100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584399-C-T

3680101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584398-T-A

3680101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584398-T-C

3680192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584307-A-G

http://identifiers.org/hco/12/GRCh38#3680468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127584090-C-A

3680468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584090-C-T

3680552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584039-A-G

3680561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127584030-C-T

3680907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127583708-C-T

http://identifiers.org/hco/12/GRCh38#3681083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127583314-C-A

3681406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127583014-G-A

http://identifiers.org/hco/12/GRCh38#3681587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127582882-A-C

3681633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127582838-C-T

http://identifiers.org/hco/12/GRCh38#3681663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127582809-A-C

3681670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127582797-A-G

3682120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 127582387-C-T

http://identifiers.org/hco/12/GRCh38#3682236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127582271-C-A

3682372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127582121-C-T

3696624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127581145-G-T

3696625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127581144-T-C

3696665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127581104-G-T

3696763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127581042-C-T

3696839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 127580966-T-C

3696891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: missense variant
orthologous variants: 127580920-C-G

3696908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: missense variant
orthologous variants: 127580903-T-G

3697074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580753-G-A

3697086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580741-G-A

3697086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580741-G-T

3697099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580728-A-G

3697099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580728-A-T

3697103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580724-G-A

3697103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580724-G-T

3697118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580709-G-A

3697118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580709-G-T

3697167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580660-T-C

3697239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580591-G-C

3697269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127580561-C-T

http://identifiers.org/hco/12/GRCh38#3697270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127580560-A-C

3704577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127579753-T-C

3705027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127578931-T-G

3705096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127578749-A-G

3705117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127578714-T-C

3705133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127578689-G-T

3707027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127577036-C-T

3707617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127576475-C-T

3710301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127574388-C-T

http://identifiers.org/hco/12/GRCh38#3713226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127573480-C-A

3713226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127573480-C-T

http://identifiers.org/hco/12/GRCh38#3713328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127573392-C-A

3713328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127573392-C-T

3713345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127573373-A-G

3713362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127573357-G-C

3713362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127573357-G-T

3713509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127573213-C-T

3713735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127573060-T-C

3714030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127572171-T-A

3714313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127571916-A-G

3714369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127571860-C-G

http://identifiers.org/hco/12/GRCh38#3714656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127571031-A-C

3714794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127570892-G-C

3714856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127570847-C-T

3714919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127570779-T-G

http://identifiers.org/hco/12/GRCh38#3717865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127568546-C-A

3717865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127568546-C-T

3718045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127568382-T-G

http://identifiers.org/hco/12/GRCh38#3718063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127568364-C-A

3718162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127568277-G-A

http://identifiers.org/hco/12/GRCh38#3719251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127568119-A-C

3719267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127568103-A-T

3719299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127568062-T-C

http://identifiers.org/hco/12/GRCh38#3719339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127568024-C-A

3719339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127568024-C-T

3719351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127568012-G-T

3719712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127567608-A-G

http://identifiers.org/hco/12/GRCh38#3719756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127567564-A-C

3719785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127567539-G-A

3719819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127567505-T-G

3720628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127567375-G-A

3720628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127567375-G-T

3720753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127567255-A-T

http://identifiers.org/hco/12/GRCh38#3720967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127567080-A-C

3721049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127567004-G-A

3721078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127566980-C-T

3722524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127564142-T-A

3722528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127564138-G-T

3722611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127564067-A-G

3722731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127563948-G-A

3722731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127563948-G-T

3722802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127563875-T-G

3722892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127563770-T-C

3722912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127563744-G-C

3723110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127563536-C-G

3723110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127563536-C-T

3723172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127563471-G-T

3723869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127562785-G-A

http://identifiers.org/hco/12/GRCh38#3723899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127562755-A-C

3724037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127562624-C-T

3724097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127562584-C-T

3724641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127562047-G-C

3724724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron variant
orthologous variants: 127561966-C-T

3725996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561807-G-T

3726070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561752-T-C

3726091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561729-T-G

3726256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561506-T-C

3726366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561409-A-T

http://identifiers.org/hco/12/GRCh38#3726397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127561379-C-A

3726546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561222-A-G

3726573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561203-A-G

3726582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561194-C-T

3726583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561193-A-G

3726594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561182-A-G

3726710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561085-C-G

3726710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561085-C-T

3726736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127561059-T-A

3727480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127560245-A-G

3727480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127560245-A-T

3727499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127560227-T-C

3727507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127560219-C-T

3727704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127560037-G-T

http://identifiers.org/hco/12/GRCh38#3727859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127559969-C-A

3728041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559886-A-G

http://identifiers.org/hco/12/GRCh38#3728046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127559884-C-A

3728046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559884-C-T

3728049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559881-A-G

3728179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559770-G-A

3728280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559665-T-C

3728299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559648-A-T

3728466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559492-A-G

http://identifiers.org/hco/12/GRCh38#3728511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127559441-C-A

3728574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559377-T-A

3728574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559377-T-C

3728625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559329-T-C

3728627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559327-G-C

3728660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559297-A-G

3728703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559279-G-A

3728703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559279-G-T

3728706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559276-T-C

http://identifiers.org/hco/12/GRCh38#3728720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127559262-A-C

3728806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559194-G-T

3728824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127559168-T-C

3728951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127559022-C-T

3728998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127558985-T-G

3729152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127558816-C-T

http://identifiers.org/hco/12/GRCh38#3729327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127558690-C-A

3729328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127558689-T-C

3729375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127558637-A-G

3729408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127558604-T-A

3729408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127558604-T-C

3729408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127558604-T-G

http://identifiers.org/hco/12/GRCh38#3730180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127557914-C-A

3730180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557914-C-T

3730194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557900-T-C

3730325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557792-A-G

3730327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557789-G-A

3730327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557789-G-T

http://identifiers.org/hco/12/GRCh38#3730555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127557562-C-A

3730555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557562-C-T

3730608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557454-T-C

3730790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557060-A-G

3730835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557017-A-G

3730841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127557011-A-G

3730863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556994-G-A

3730863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556994-G-T

3731019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556870-G-T

3731122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556767-A-G

3731122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556767-A-T

http://identifiers.org/hco/12/GRCh38#3731357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127556701-C-A

3731357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556701-C-G

3731357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556701-C-T

3731372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556694-C-T

http://identifiers.org/hco/12/GRCh38#3731427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127556651-C-A

3731427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556651-C-T

http://identifiers.org/hco/12/GRCh38#3731521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127556558-C-A

3731521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556558-C-T

http://identifiers.org/hco/12/GRCh38#3731562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127556517-C-A

3731562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556517-C-T

3731577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556500-T-C

3731603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556474-T-C

3731662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556402-G-T

3731706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556336-T-C

3731905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127556089-C-T

http://identifiers.org/hco/12/GRCh38#3731966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127556017-C-A

http://identifiers.org/hco/12/GRCh38#3732124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127555892-C-A

3732124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555892-C-T

3732142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555874-C-T

3732289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555744-G-T

3732407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555619-A-G

3732428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555595-T-C

http://identifiers.org/hco/12/GRCh38#3732459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127555561-C-A

3732459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555561-C-T

http://identifiers.org/hco/12/GRCh38#3732501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127555519-C-A

3732519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555501-T-G

http://identifiers.org/hco/12/GRCh38#3732573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127555474-C-A

3732573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555474-C-T

http://identifiers.org/hco/12/GRCh38#3732605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127555458-C-A

3732680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555384-A-G

3732689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555375-C-T

3732749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555315-A-G

3732759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555305-G-A

3732760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555304-G-T

3732783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555283-C-T

3732794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555271-C-T

http://identifiers.org/hco/12/GRCh38#3732996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127555042-C-A

3733053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555002-G-A

3733053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127555002-G-T

3733108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127554919-G-A

3733108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 127554919-G-T

3733241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127554820-C-G

3733241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127554820-C-T

3733318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127554706-A-G

3733410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127554618-G-A

3738932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127551210-G-A

http://identifiers.org/hco/12/GRCh38#3739046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127551129-C-A

3739046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127551129-C-T

3739215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550998-T-C

3739497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550766-G-A

3739552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550722-T-C

3740028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550533-G-A

3740098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550490-T-C

3740182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550395-C-T

3740200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550381-G-A

3740475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550198-T-G

3740498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127550175-T-C

3740823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127549456-C-T

3741038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127549284-T-A

3741080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127549242-T-C

3741093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127549229-C-T

3741189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127549144-C-T

3741293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127549065-G-A

http://identifiers.org/hco/12/GRCh38#3741329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127549029-C-A

3741364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127548994-C-T

3741504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127548711-T-C

3741793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127548443-C-G

3741864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127548365-A-G

http://identifiers.org/hco/12/GRCh38#3741877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127548348-A-C

3742036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127548171-G-A

3743540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127547962-G-A

3743597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127547910-C-T

3743754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127547759-G-C

3743766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127547748-G-C

3743799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127547714-C-T

3743821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127547680-A-G

3744355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127547180-C-T

3744474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127547065-G-T

3745162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127546621-G-T

3745288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127546525-T-C

3745349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127546483-C-T

3745367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127546460-C-T

3745405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127546427-G-A

3745465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127546367-T-C

3746739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545755-G-A

http://identifiers.org/hco/12/GRCh38#3746745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127545750-C-A

3747233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545340-G-A

3747251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545322-T-C

3747259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545314-G-A

http://identifiers.org/hco/12/GRCh38#3747281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127545290-C-A

3747281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545290-C-T

http://identifiers.org/hco/12/GRCh38#3747440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127545183-C-A

3747440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545183-C-T

3747441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545182-G-A

3747441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545182-G-T

3747546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127545097-G-T

3747726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127544916-T-C

3748685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127543199-G-C

3748990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127542996-C-T

3749068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127542903-A-G

http://identifiers.org/hco/12/GRCh38#3749090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127542885-C-A

3749559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127542027-C-T

3749573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127542013-G-A

3749573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127542013-G-C

3749573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127542013-G-T

3749648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127541936-C-T

3749742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127541840-T-C

3750383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127540999-G-A

3750520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127540900-C-T

3750563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127540861-G-A

3750695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127540758-G-A

3751171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127540088-T-C

http://identifiers.org/hco/12/GRCh38#3751422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127539865-A-C

3751422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539865-A-T

3751487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539813-G-A

3751592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539711-C-G

3751637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539676-C-T

3751773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539542-C-T

3751919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539430-T-A

3751919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539430-T-C

3752006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539346-C-T

3752032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539320-G-C

3752138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127539211-G-A

3752375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538980-C-G

3752375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538980-C-T

3752426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538923-G-C

3752426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538923-G-T

3752763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538596-A-G

3752788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538573-T-G

3752818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538552-G-A

3752818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538552-G-C

3752867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538504-C-T

3752904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127538468-G-C

3752942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127538427-G-A

3752942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127538427-G-T

http://identifiers.org/hco/12/GRCh38#3753044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127538358-C-A

3753044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127538358-C-T

http://identifiers.org/hco/12/GRCh38#3753059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127538336-C-A

3753059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127538336-C-G

3753059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127538336-C-T

3753163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127538244-C-T

3753214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127538196-G-A

3753214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127538196-G-T

http://identifiers.org/hco/12/GRCh38#3753265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127538136-C-A

3753265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538136-C-G

3753265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538136-C-T

3753316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538089-C-T

3753346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538041-A-G

3753346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127538041-A-T

3753469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127537925-G-A

3753663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127537768-C-G

3753663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127537768-C-T

3753882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127537567-G-A

3753882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127537567-G-C

3754320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127537075-G-C

3754321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127537074-C-T

3754354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127537038-C-T

3754392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127537000-G-A

3754419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127536979-T-C

3754504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127536884-C-G

3754537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127536848-T-C

3754977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127535116-C-T

3755179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127534957-G-A

3755179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127534957-G-T

3755294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127534857-C-T

3755305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127534846-C-T

3755334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127534817-G-T

3755852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127534559-T-C

3756175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127534237-T-G

3756474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127533968-T-C

3756498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127533956-G-A

3756595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127533877-A-T

3756742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127533670-G-T

3757256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127532858-G-A

3757323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127532797-A-G

3757381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127532738-A-G

3757463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127532668-A-G

3757511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127532635-C-T

http://identifiers.org/hco/12/GRCh38#3757578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127532552-C-A

3757578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127532552-C-T

3757606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127532518-G-T

3757747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127532389-G-A

3757788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127532351-G-A

3757788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127532351-G-C

3757800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127532339-G-A

3758971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127530305-C-T

3759011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127530266-T-C