46921189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71721730-G-A

46921364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71721896-C-T

http://identifiers.org/hco/4/GRCh38#46921453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71721988-C-A

46921521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722035-C-T

46921589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722103-T-C

46921877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722394-G-A

46921939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722459-G-A

46922115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722623-G-T

46922220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722730-G-A

46922237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722747-C-T

46922264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722774-T-C

46922336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722834-C-T

46922351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722849-C-T

46922377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722875-T-C

http://identifiers.org/hco/4/GRCh38#46922390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71722888-C-A

46922390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71722888-C-T

46923522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71724418-T-C

46923609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71724497-G-A

http://identifiers.org/hco/4/GRCh38#46923680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71724547-C-A

46923680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71724547-C-T

46923877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71724753-C-T

46923922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71724780-A-T

http://identifiers.org/hco/4/GRCh38#46923939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71724797-C-A

46924248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725064-C-T

http://identifiers.org/hco/4/GRCh38#46924382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71725145-C-A

http://identifiers.org/hco/4/GRCh38#46924534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71725279-C-A

46924740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725459-C-T

46924749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725465-T-C

46924840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725558-T-A

46924840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725558-T-C

46924864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725572-T-C

46924939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725633-A-G

46925125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725822-A-G

46925255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725950-T-C

46925296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71725985-T-C

46925334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71726022-A-G

46925385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71726072-G-A

46925424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71726111-T-C

46925446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71726147-G-A

46925849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71726477-T-C

46925862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71726489-G-A

46926225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727056-G-A

46926641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727442-A-G

46926806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727604-G-A

http://identifiers.org/hco/4/GRCh38#46926992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71727786-C-A

46927043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727837-G-A

46927043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727837-G-T

46927126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727917-G-A

46927138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727929-G-A

46927138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727929-G-T

http://identifiers.org/hco/4/GRCh38#46927153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71727944-A-C

46927153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71727944-A-G

46927750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728556-T-C

46927860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728665-G-C

46927860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728665-G-T

46927934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728746-T-C

46927935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728747-G-T

http://identifiers.org/hco/4/GRCh38#46927936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71728748-C-A

46927936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728748-C-G

46927936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728748-C-T

http://identifiers.org/hco/4/GRCh38#46927938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71728750-C-A

46927938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728750-C-T

http://identifiers.org/hco/4/GRCh38#46927953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71728765-A-C

http://identifiers.org/hco/4/GRCh38#46928055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71728872-C-A

46928055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728872-C-G

46928055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3 prime UTR variant
orthologous variants: 71728872-C-T

http://identifiers.org/hco/4/GRCh38#46928194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71729012-C-A

46928303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71729120-T-C

46928487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 71729304-G-T

46928549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71729363-T-C

46928585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71729399-T-C

http://identifiers.org/hco/4/GRCh38#46928644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71729458-C-A

46928644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 71729458-C-G

46928644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 71729458-C-T

46928831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71729639-T-C

46928882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71729689-T-A

46928882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71729689-T-C

http://identifiers.org/hco/4/GRCh38#46930040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71729963-A-C

46930041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71729964-G-A

46930047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71729970-T-C

46930205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71730145-T-C

46930468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71730342-G-T

http://identifiers.org/hco/4/GRCh38#46930556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71730433-C-A

46930634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71730672-C-T

http://identifiers.org/hco/4/GRCh38#46930815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71730926-C-A

46930815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71730926-C-T

http://identifiers.org/hco/4/GRCh38#46930830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71730941-C-A

46930895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71731004-C-T

46930952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71731063-A-T

46931092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71731200-G-C

46931628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738211-T-A

46931667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738249-C-T

46931668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738250-G-A

46932111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738643-T-C

46932384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738905-T-C

46932401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738924-C-G

46932401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738924-C-T

46932480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738958-A-G

46932493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738970-C-G

46932493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71738970-C-T

46932659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71739163-T-G

46933037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71739800-T-C

46933067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71739831-T-C

46933094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71739858-G-A

46933094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71739858-G-T

46933096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71739860-G-A

46933096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71739860-G-C

46933257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71740010-C-T

46933562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71740307-T-C

46933654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71740587-C-G

46933654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71740587-C-T

46933695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71740629-C-T

46934463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71741392-C-G

46934516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71741442-T-C

46934564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71741490-G-A

46934707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71741628-C-T

46934729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71741650-G-A

46934729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71741650-G-T

46935029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71741989-A-G

46935054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71742014-T-C

46935086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71742044-G-A

46935244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71742183-A-G

46935368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71742302-G-A

46936685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71742841-A-G

46936981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71743082-A-G

46936982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71743083-C-G

46936982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71743083-C-T

46937591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71747909-C-T

46937662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71747978-G-T

46937927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71748219-C-T

46938008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71748265-G-T

46938169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71749510-T-C

46938181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71749522-G-A

46938210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71749550-T-C

46938262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71749603-A-G

46938353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71749693-T-C

46938387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71749726-T-C

46938673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71749965-A-G

46938769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750053-G-C

46939005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750314-G-T

46939092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750378-T-C

46939128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750419-C-T

46939231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750514-T-C

46939435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750728-G-A

46939488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750769-T-A

46939488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750769-T-C

46939539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750817-T-A

46939539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750817-T-C

46939574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750851-G-A

46939597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750874-T-C

46939635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750893-T-A

46939674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71750929-A-G

46939772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71751039-C-T

46940095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71751484-C-T

46940250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71751638-T-G

46940459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71751912-G-A

46940459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71751912-G-C

46940515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71751968-G-C

46940692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71752816-C-T

46940830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71752930-G-A

46940830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71752930-G-T

http://identifiers.org/hco/4/GRCh38#46940874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71752974-C-A

http://identifiers.org/hco/4/GRCh38#46941402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71753519-A-C

46941450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71753555-G-A

46941469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71753574-T-C

46941554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71753643-G-A

46941590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71753671-A-G

46941640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71753720-A-G

46944665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71759281-T-C

46944762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71759380-T-C

46945225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71759829-C-G

http://identifiers.org/hco/4/GRCh38#46945327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71759921-C-A

46945327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71759921-C-T

46945426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760018-C-G

46945426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760018-C-T

46945935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760515-G-A

46945935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760515-G-C

46945975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760552-G-A

46946007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760584-T-G

http://identifiers.org/hco/4/GRCh38#46946073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71760647-C-A

46946073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760647-C-T

46946183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760756-C-T

46946205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760778-T-C

46946259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760832-T-A

46946259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71760832-T-C

http://identifiers.org/hco/4/GRCh38#46946489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71761066-C-A

46946611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71761190-C-T

46946689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71761269-T-C

46946691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71761271-G-T

46946934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71761487-T-A

46947206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71761765-T-G

46947564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762125-G-A

46947627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762167-T-G

46947645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762186-G-A

46947669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762196-C-G

46947756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762281-A-G

46947756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762281-A-T

46947840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762359-T-A

46947840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762359-T-C

http://identifiers.org/hco/4/GRCh38#46947845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71762364-A-C

46947933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762423-T-C

46947988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762479-G-C

46948069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71762566-C-T

http://identifiers.org/hco/4/GRCh38#46948987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71763461-A-C

46949062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71763522-T-C

46949062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71763522-T-G

46949076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71763537-G-C

46949130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71763687-T-A

46949278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71763844-T-C

46949526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71763937-T-C

46949646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71763994-A-T

46949680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71764029-T-C

46949710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71764058-G-A

http://identifiers.org/hco/4/GRCh38#46949743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71764091-A-C

46949745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71764093-G-A

http://identifiers.org/hco/4/GRCh38#46950255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71764581-C-A

46950419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71764742-A-T

46950466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71764785-G-A

46950553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71764874-G-A

46950576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71764897-A-G

46950576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71764897-A-T

46950754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71765065-T-A

46950799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71765109-T-C

46950847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71765156-T-G

46951057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71765334-A-G

46951122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71765400-G-A

http://identifiers.org/hco/4/GRCh38#46951347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71765599-A-C

46952246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71765912-T-C

46952290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71765957-G-A

46952379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71766042-C-T

46952830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71766496-G-A

46953266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71766886-C-G

46953465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767086-T-C

46953523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767148-T-C

46953572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767195-G-A

46953618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767239-T-C

46953720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767326-A-T

46953852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767455-A-G

46954048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767637-G-A

46954048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767637-G-T

46954253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767827-C-G

46954698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767968-T-C

46954724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71767994-A-T

46954784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71768046-G-A

46954826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71768086-C-T

46955078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71768572-T-C

46955406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71768903-T-C

46955452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71768950-C-T

http://identifiers.org/hco/4/GRCh38#46955801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71769305-A-C

46955842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71769347-A-G

46956258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71769665-G-T

46956285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71769692-T-C

46956415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71769855-T-C

46956449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71769889-A-G

46956461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71769899-G-A

46956577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71770078-C-T

46956628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71770133-C-T

46957074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71770857-A-G

46957379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71771171-T-C

http://identifiers.org/hco/4/GRCh38#46957406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71771197-C-A

46957607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71771370-G-C

46957723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71771485-T-C

46958169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71772382-T-C

46958568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71773015-A-G

46958751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71773206-T-C

46958768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71773223-C-T

46958811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71773263-C-T

46958956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71773747-T-A

46959025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71773816-C-T

46959281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774034-C-T

46959329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774081-T-C

46959403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774145-C-T

46959469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774208-T-C

46959600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774332-T-A

46959600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774332-T-G

46959707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774394-G-C

http://identifiers.org/hco/4/GRCh38#46959787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71774481-C-A

46959801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774498-T-A

46959802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774499-A-G

46959831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774552-T-G

46959832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774553-A-G

46959832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774553-A-T

46959834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774554-A-G

46959834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774554-A-T

46959842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774565-G-A

46959880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774613-C-G

46959920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774652-T-C

46959946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774678-T-C

46960011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71774780-G-A

46960498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71775323-G-T

46960626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71775433-T-C

46960721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71775492-T-C

46960760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71775531-A-G

46960805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71775569-C-G

46960852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71775615-G-T

46964976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71781204-A-G

46965069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71781297-A-G

46965183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71781411-T-C

http://identifiers.org/hco/4/GRCh38#46965335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71781557-C-A

46965336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71781558-A-G

46965558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71781772-A-G

46965617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71782014-C-T

46965762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71782611-G-A

46966017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71782844-C-T

46966024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71782851-G-A

46966024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71782851-G-C

46966250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71783077-A-T

46966252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71783079-A-G

46966339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71783153-T-C

46966436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71783252-G-T

46966637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71783620-T-C

46966817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71783810-C-G

http://identifiers.org/hco/4/GRCh38#46967030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71784227-A-C

46967032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784229-G-A

http://identifiers.org/hco/4/GRCh38#46967048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71784245-A-C

46967048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784245-A-T

46967101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784300-A-G

46967123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784322-G-A

46967123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784322-G-T

46967224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784611-A-G

http://identifiers.org/hco/4/GRCh38#46967254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71784638-C-A

46967254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784638-C-T

46967276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784660-A-G

46967303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784687-G-C

46967303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784687-G-T

46967319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71784703-T-C

46967641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71785100-A-G

46968140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71785617-C-T

http://identifiers.org/hco/4/GRCh38#46968239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71785713-C-A

46968239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71785713-C-T

46968638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71786103-G-A

46968638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71786103-G-C

46968771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71786247-C-T

46969827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71788766-T-C

46970218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71789623-G-A

46970483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71789885-C-T

46970540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71790362-C-T

46970551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71790373-A-G

http://identifiers.org/hco/4/GRCh38#46971216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71791022-C-A

46971216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71791022-C-T

46971266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71791069-T-C

46971268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71791071-G-A

46971268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71791071-G-C

46971268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71791071-G-T

46971292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71791095-G-C

46971292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71791095-G-T

46971384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71791153-T-G

46972337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71792937-C-G

46972530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71793131-A-G

http://identifiers.org/hco/4/GRCh38#46973137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71793746-C-A

46973137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71793746-C-T

46973205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71793816-T-C

46973540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71794270-G-A

46973968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71794628-T-C

46974134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71794769-T-C

46974569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71795780-G-A

46975221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796438-A-G

46975264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796481-T-C

46975275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796508-A-G

46975330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796556-T-A

46975569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796814-C-T

46975586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796832-G-C

46975586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796832-G-T

http://identifiers.org/hco/4/GRCh38#46975659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71796909-C-A

http://identifiers.org/hco/4/GRCh38#46975671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71796921-C-A

46975688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796935-C-T

46975734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71796979-A-G

46975861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71797110-C-T

46976034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71797285-T-A

46976034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71797285-T-C

46976146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71797396-G-T

46976334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71797571-G-C

46976334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71797571-G-T

46976405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71797610-A-G

http://identifiers.org/hco/4/GRCh38#46976579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71797789-C-A

46976958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798069-G-T

http://identifiers.org/hco/4/GRCh38#46977005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71798115-A-C

46977122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71798232-A-G

46977259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798352-A-G

46977259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798352-A-T

46977324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798378-G-A

46977324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798378-G-T

46977326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798380-G-A

46977326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798380-G-C

46977326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798380-G-T

46977565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71798561-G-A

46977739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798721-T-C

46977739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798721-T-G

46977762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798744-G-A

46977767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798749-G-T

46977825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798803-T-G

http://identifiers.org/hco/4/GRCh38#46977861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71798844-A-C

46977951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71798933-G-A

46978149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799140-G-A

46978149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799140-G-T

46978151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799142-C-T

46978182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799169-G-A

46978182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799169-G-C

46978801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799416-T-G

http://identifiers.org/hco/4/GRCh38#46979120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71799691-A-C

46979120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799691-A-G

46979120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799691-A-T

46979154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799725-G-A

46979154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799725-G-T

46979333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71799994-T-C

46979469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71800133-G-A

46979503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71800169-C-T

46979807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71800470-C-T

46979890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71800533-A-G

46980225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801086-G-A

46980390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801219-G-A

http://identifiers.org/hco/4/GRCh38#46980392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71801221-C-A

46980392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801221-C-G

http://identifiers.org/hco/4/GRCh38#46980488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71801310-C-A

46980488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801310-C-G

46980565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801387-G-C

46980593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801420-T-A

46980666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801486-T-C

46980667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801487-T-C

http://identifiers.org/hco/4/GRCh38#46980757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71801571-C-A

46980857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801664-T-C

46980912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801708-T-C

46980997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801798-T-C

46981146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71801947-A-T

46981316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71802128-T-C

46981402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71802211-A-T

46981534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71802342-G-A

46981684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71802452-G-A

46982276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71802990-G-T

46982391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71803115-A-T

46982597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71803281-T-C

46982612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71803293-T-C

46983031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71803701-T-A

46983066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71803732-T-C

46983094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71803759-A-G

46983738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71804368-C-T

http://identifiers.org/hco/4/GRCh38#46983920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71804579-C-A

46983920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71804579-C-G

46983920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71804579-C-T

http://identifiers.org/hco/4/GRCh38#46984017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71804654-A-C

46984327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71804937-C-T

46984519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805165-T-C

46984764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805381-A-G

46984931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805638-A-G

46984949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805656-C-T

46985015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805745-C-G

46985094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805823-T-C

46985248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805977-G-A

46985265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805993-T-A

46985265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71805993-T-G

46985523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71806219-T-C

46985526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71806222-C-G

46986566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71808713-T-C

http://identifiers.org/hco/4/GRCh38#46986606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71808761-C-A

46986863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809011-C-T

46986898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809046-A-G

http://identifiers.org/hco/4/GRCh38#46986913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71809063-C-A

46986913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809063-C-G

46986977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809127-C-T

46987006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809152-T-A

http://identifiers.org/hco/4/GRCh38#46987048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71809197-C-A

46987048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809197-C-G

46987048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809197-C-T

46987070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809224-T-A

46987070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809224-T-G

46987292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809422-T-C

46987519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809630-C-G

46987795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809896-T-C

46987880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809959-T-C

46987904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71809983-T-C

46988343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71810445-C-T

46988437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71810525-G-T

46988464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71810562-T-G

46988761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71810817-G-A

46988761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71810817-G-T

46988804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71810860-T-C

http://identifiers.org/hco/4/GRCh38#46988820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71810877-C-A

46988955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71811007-G-A

http://identifiers.org/hco/4/GRCh38#46989065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71811125-A-C

46989785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71811811-T-C

46990042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71812074-C-G

46990590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71812648-A-G

46990846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71812933-C-T

http://identifiers.org/hco/4/GRCh38#46991091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71812987-C-A

46991176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813020-A-G

46991623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813385-A-G

46991623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813385-A-T

46991736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813472-C-T

46991738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813474-G-A

46991823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813554-G-C

46992165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813848-A-G

46992165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813848-A-T

46992255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71813936-G-A

46992472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71814143-T-C

46992531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71814214-G-A

46992531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71814214-G-T

http://identifiers.org/hco/4/GRCh38#46992575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71814250-C-A

46992575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71814250-C-G

46992575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71814250-C-T

46992734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71814427-G-T

46992769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71814459-A-G

46992769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71814459-A-T

46992786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71814471-G-T

http://identifiers.org/hco/4/GRCh38#46992809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71814494-C-A

46992809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71814494-C-T

http://identifiers.org/hco/4/GRCh38#46993268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71814976-C-A

46993268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71814976-C-T

46993579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71815322-T-A

46993579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4078
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71815322-T-C