19682247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786470-T-C

19682247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786470-T-G

http://identifiers.org/hco/1/GRCh38#19682272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138786453-C-A

http://identifiers.org/hco/1/GRCh38#19682314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138786437-C-A

19682385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786362-G-C

19682394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786356-A-G

19682428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786316-T-C

19682430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786314-T-A

19682430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786314-T-C

19682434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786310-T-C

19682451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786295-G-T

19682585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786173-G-A

19682585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138786173-G-C

19682768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138786030-T-C

http://identifiers.org/hco/1/GRCh38#19682805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138786003-C-A

19682805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138786003-C-T

19682807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138786001-G-A

19682807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138786001-G-T

19682926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138785936-A-T

19683000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138785863-T-C

19683077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138785788-G-A

19683279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138785583-G-A

19683328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138785537-G-A

19683331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138785534-C-T

19683364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138785501-G-A

19683364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138785501-G-C

19683364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138785501-G-T

19683422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138785443-G-A

19683454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785410-A-G

19683454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785410-A-T

http://identifiers.org/hco/1/GRCh38#19683493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138785368-C-A

19683493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785368-C-T

19683495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785366-T-C

http://identifiers.org/hco/1/GRCh38#19683602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138785297-A-C

19683602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785297-A-T

19683613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785286-G-A

19683658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785240-T-C

19683682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785217-T-A

19683688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138785211-C-T

19687595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138783704-T-C

19687764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138783543-G-A

http://identifiers.org/hco/1/GRCh38#19687892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138783446-C-A

19687918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138783420-C-G

19687918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138783420-C-T

http://identifiers.org/hco/1/GRCh38#19688094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138783275-C-A

19688679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138782667-C-G

19688861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138782334-C-T

19688862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138782333-T-C

19689020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138782183-C-T

19689373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138781902-C-T

19689387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138781888-C-T

19694414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138781346-A-G

http://identifiers.org/hco/1/GRCh38#19694552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138781208-C-A

19694552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 138781208-C-T

19694628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138781153-T-C

19694637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138781141-A-G

19700213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780360-G-T

http://identifiers.org/hco/1/GRCh38#19700277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138780310-C-A

19700277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780310-C-T

19700454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780182-G-A

19700565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780116-T-C

19700628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780054-A-T

http://identifiers.org/hco/1/GRCh38#19700644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138780043-C-A

19700644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780043-C-T

19700715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779980-T-C

19700720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779975-G-T

19700846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138779849-G-A

19700919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138779776-C-T

http://identifiers.org/hco/1/GRCh38#19700928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138779767-C-A

19700945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138779748-G-C

19700945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138779748-G-T

http://identifiers.org/hco/1/GRCh38#19700995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138779688-C-A

http://identifiers.org/hco/1/GRCh38#19701080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138779625-A-C

19701080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138779625-A-G

19701125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138779588-T-A

19701139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138779574-G-T

19704390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138777641-A-T

19704467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138777562-A-T

19704468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138777561-C-T

19704473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138777556-A-T

19704550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138777404-G-A

19704631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138777236-G-T

http://identifiers.org/hco/1/GRCh38#19704641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138777226-C-A

19704641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138777226-C-T

19704903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138776963-C-T

19706224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138776772-C-T

19708331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774722-C-T

19708481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774617-C-G

19708865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774360-A-G

19708988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774235-T-C

19709022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774199-G-A

19709022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774199-G-C

19709032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774189-T-C

19709066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774159-G-A

19709203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774021-G-A

19709349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138773901-C-G

19709694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138773547-G-A

http://identifiers.org/hco/1/GRCh38#19710361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138772888-C-A

19710373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772876-A-G

19710444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772825-T-C

19710599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772714-T-G

19710668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772650-T-G

19715459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138768691-G-A

19715608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138768558-T-A

19715608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138768558-T-C

19725134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765941-C-T

19725318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765771-T-G

http://identifiers.org/hco/1/GRCh38#19725515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138765520-A-C

19725522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765512-C-T

http://identifiers.org/hco/1/GRCh38#19725598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138765434-C-A

19725679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765380-C-T

http://identifiers.org/hco/1/GRCh38#19725689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138765370-A-C

19725690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765369-T-C

http://identifiers.org/hco/1/GRCh38#19725928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138765160-C-A

19726028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765065-C-T

19727516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138764913-C-T

19728520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138764277-T-A

19728554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138764243-C-T

19728624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138764175-T-C

19728869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763971-A-G

19730909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763321-T-A

19731385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763041-T-C

19731586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762858-G-C

19731661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762786-T-C

19731825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762654-C-T

19731917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762578-G-C

19731974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762518-A-G

19732075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762440-T-A

19732075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762440-T-G

19733717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762144-A-G

http://identifiers.org/hco/1/GRCh38#19733865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138762028-C-A

19733933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761965-T-C

19733997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761923-T-C

19734052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761883-C-G

19734428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761606-G-A

http://identifiers.org/hco/1/GRCh38#19734429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138761605-C-A

19734433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761601-G-A

http://identifiers.org/hco/1/GRCh38#19734435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138761599-A-C

19734490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761544-C-T

19734574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761498-G-A

19734666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761408-G-A

19734841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761237-T-C

http://identifiers.org/hco/1/GRCh38#19734959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138761113-C-A

19735091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138761003-T-C

19735404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138760689-T-C

19735783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138760151-T-C

19736042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138759943-T-C

19736042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138759943-T-G

19736066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138759910-A-G

19736621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138758161-C-G

19737398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138757196-C-T

http://identifiers.org/hco/1/GRCh38#19737498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138757096-C-A

19737498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138757096-C-T

19737577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138757042-G-T

19737593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138757027-T-C

19737598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138757022-G-A

19737640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138756980-T-C

19737696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138756930-C-T

19737751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138756877-C-T

19737809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138756821-G-A

http://identifiers.org/hco/1/GRCh38#19739685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138750523-C-A

19739685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750523-C-G

19739685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750523-C-T

19739687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750521-G-A

19739687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750521-G-C

19739687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750521-G-T

19739717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750491-G-T

19739729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750480-A-G

19739729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750480-A-T

19739730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750479-G-C

19739760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750449-A-G

19739781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750418-C-G

19739781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750418-C-T

19739798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750397-A-G

19739873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138750327-G-A

19739915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138750285-G-A

19739915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138750285-G-C

19739969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750231-G-C

19739987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750208-G-C

19740042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750149-A-T

19740183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138749995-C-T

19740631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138749221-A-G

19740652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138749199-C-T

19740653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138749198-T-A

19740653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138749198-T-C

http://identifiers.org/hco/1/GRCh38#19740983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138748881-C-A

19740983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748881-C-G

19744950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748846-G-C

19745025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748773-T-C

19745045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748753-C-G

19745050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748748-G-A

19745054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748744-G-A

19745098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748700-G-A

19745189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748609-T-C

19745210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748596-G-A

19745221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748585-A-G

19745224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748582-G-A

19745236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748574-G-A

19745266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748544-G-A

19745305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748517-T-G

19745335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748487-G-T

19745380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748438-G-T

19745381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748437-A-G

http://identifiers.org/hco/1/GRCh38#19745387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138748433-C-A

19745387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748433-C-T

19745388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748432-C-T

19745482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 138748345-C-T

19745495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 138748332-C-G

19745495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 138748332-C-T

http://identifiers.org/hco/1/GRCh38#19745501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138748326-C-A

19745501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 138748326-C-T

19745668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748151-G-A

19745740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748124-G-C

http://identifiers.org/hco/1/GRCh38#19745758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138748111-C-A

19745758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748111-C-G

19745758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748111-C-T

19746087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747860-G-A

19746087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747860-G-C

19746371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747583-G-T

http://identifiers.org/hco/1/GRCh38#19746385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138747566-C-A

19746385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747566-C-T

19746412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747542-T-C

19746488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138747466-G-A

19746500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138747454-G-A

19746566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138747388-G-A

19747029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747068-T-C

19747034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747063-G-T

19747036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747060-C-T

19747060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747037-C-T

19747078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747026-G-A

19747078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747026-G-C

19747078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138747026-G-T

19747152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138746991-G-C

http://identifiers.org/hco/1/GRCh38#19747162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138746980-C-A

19747162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 138746980-C-G

19747162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 138746980-C-T

19747170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138746972-C-G

19747170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138746972-C-T

19747207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138746935-T-A

19747207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138746935-T-C

19747275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138746868-G-A

19747275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138746868-G-T

19747351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138746790-G-T

19747466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138746729-T-G

http://identifiers.org/hco/1/GRCh38#19747557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138746601-A-C

19747645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138746549-C-T

19749005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138745085-T-A

19749005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138745085-T-C

19749061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138745038-T-C

19749602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744357-A-G

19749659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744291-T-G

19749732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744221-C-T

19749782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744170-G-A

19749817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744135-T-A

19749843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744113-C-T

19749928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744035-A-G

http://identifiers.org/hco/1/GRCh38#19749970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138743999-C-A

19749970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743999-C-T

19750156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743816-G-T

http://identifiers.org/hco/1/GRCh38#19750264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138743720-A-C

19750264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743720-A-G

19750274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743697-C-T

19750283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743688-G-A

19750283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743688-G-T

19750288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743683-T-C

19750301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743671-C-T

http://identifiers.org/hco/1/GRCh38#19750313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138743659-C-A

19750313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743659-C-G

19750392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743567-G-A

19751166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743488-C-T

19752118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

19752253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-G

19752253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-T

19752312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-T

19752385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-T

19752444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

19752448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

19752503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

19752506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

19753285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138740780-G-A

19753304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138740761-C-T

19753431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138740637-G-A

19753441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138740627-G-T

19753527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138740547-G-A

19754141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138740140-G-T

19754232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138740047-G-T

19755403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138738149-C-T

19755451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138738100-C-G

19755495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138738053-G-T

19755507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138738044-G-T

19755562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138737989-G-T

19755622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138737922-G-A

19755622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138737922-G-C

19755651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138737893-G-A

19755651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138737893-G-C

http://identifiers.org/hco/1/GRCh38#19755652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138737892-A-C

19755837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138737711-C-T

19755856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138737686-A-G

19757361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138736497-G-A

19757710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138736186-T-C

19757809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138736085-T-C

19757943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138735999-G-A

19758200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138735765-G-A

19758213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138735752-G-T

19758215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138735750-A-G

19758314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138735648-C-T

19758474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138735508-C-T

19758702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138735343-A-G

19758737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138735316-G-A

http://identifiers.org/hco/1/GRCh38#19758749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138735305-A-C

19758855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138735193-C-T

19759354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138734787-T-C

19759494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138734649-G-T

19759884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138734368-G-A

19760302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138734097-C-T

19760837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138733646-G-A

19760864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138733621-T-A

19760937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138733562-T-A

19764872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138731874-T-A

19764872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138731874-T-G

19764936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138731812-C-T

19765366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138731410-G-A

19765471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138731058-G-C

19765573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138730963-A-T

19765575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138730961-C-T

19765595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138730939-T-C

19765598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138730936-G-A

19765846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138730711-G-A

19766029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730543-C-T

19766074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730508-G-A

19766103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730485-T-G

19766107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730481-C-G

19766135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730465-C-G

19766135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730465-C-T

19766147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730453-T-C

19766192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730405-T-C

19766196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138730401-C-T

19769946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725818-T-C

19769948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725816-G-A

19770081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725679-T-C

19770189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725594-G-C

19770213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725578-G-A

19770271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725519-A-G

http://identifiers.org/hco/1/GRCh38#19770409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138725438-C-A

19770608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725294-T-C

19770623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725280-G-A

19770623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725280-G-T

19770653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725246-G-A

19770665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725241-G-A

19770665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725241-G-C

19770665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725241-G-T

19770700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725207-T-G

http://identifiers.org/hco/1/GRCh38#19770708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138725199-A-C

19770708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725199-A-G

19770732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138725175-G-C

19771050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138724877-C-T

http://identifiers.org/hco/1/GRCh38#19771331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138723858-C-A

19771331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138723858-C-T

19771375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138723814-G-T

19771387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138723802-C-G

19771387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138723802-C-T

19771408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138723781-G-A

http://identifiers.org/hco/1/GRCh38#19771551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138723640-A-C

19771551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723640-A-T

19771552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723639-G-C

19771552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723639-G-T

19771554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723637-T-C

19771554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723637-T-G

19771600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723610-G-A

19771600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723610-G-T

19771601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723609-T-A

19771601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723609-T-C

http://identifiers.org/hco/1/GRCh38#19771618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138723592-A-C

19772222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723414-C-T

19772551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138723185-C-T

19772935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138722908-A-T

19773717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138722436-T-A

19774160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138722078-T-C

19774160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138722078-T-G

19774304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138721938-G-C

19774481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138721769-T-C

19778717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719204-T-C

19778742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719180-C-T

19778888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719049-G-T

19778960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718975-A-G

http://identifiers.org/hco/1/GRCh38#19779239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138718826-C-A

19779239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718826-C-T

19779273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718794-G-A

19779329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718740-A-G

19779366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718705-T-C

19779428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718675-C-T

http://identifiers.org/hco/1/GRCh38#19779465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138718650-A-C

19779529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718587-C-T

19779571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718545-T-C

http://identifiers.org/hco/1/GRCh38#19779661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138718461-A-C

19779706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718429-G-C

19779831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138718312-G-C

19780780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138717839-T-C

19780805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138717816-G-A

19780805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138717816-G-T

http://identifiers.org/hco/1/GRCh38#19783286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138714794-C-A

19783449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138714626-G-C

http://identifiers.org/hco/1/GRCh38#19783572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138714438-A-C

19783617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138714393-C-T

19783670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138714340-G-A

19783807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138714198-G-T

19783840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138714165-C-T

19783943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138714061-T-C

19786381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711728-G-A

19786841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711268-G-A

19786841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711268-G-C

19786939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711166-G-A

19786992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711107-G-A

19787066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138711029-A-G

19787325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138710835-G-C

19787428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138710761-G-A

19787493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138710677-C-T

19787518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138710665-A-G

19787621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138710592-G-A

19788325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138708633-T-A

19788434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138708532-C-T

19788461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138708502-G-A

19788467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138708496-A-G

19791619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138706801-G-A

19792315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138706498-C-G

http://identifiers.org/hco/1/GRCh38#19792410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138706405-A-C

19792500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138706313-G-A

19792541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138706281-T-C

19792609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138706212-T-C

19792684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138706121-G-T

http://identifiers.org/hco/1/GRCh38#19792759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138706063-A-C

19792761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138706061-G-T

19792950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138705916-T-C

19792960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138705906-A-T

19793067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138705811-G-T

19793716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138705209-A-G

19793903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138705031-A-G

19796063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704783-C-G

19796163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704667-G-A

19796211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704620-G-A

19796323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704424-T-C

19797479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138703541-A-G

19798035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138703450-G-A

19798148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138703356-G-A

19798148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138703356-G-T

http://identifiers.org/hco/1/GRCh38#19798155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138703349-C-A

19798155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138703349-C-T

19798170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138703340-C-T

19798176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138703334-C-G

http://identifiers.org/hco/1/GRCh38#19798178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138703332-C-A

19798875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701256-A-G

19798941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701208-A-G

19798943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701206-G-A

19798988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701185-G-A

http://identifiers.org/hco/1/GRCh38#19799112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138701083-C-A

19799112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701083-C-T

http://identifiers.org/hco/1/GRCh38#19799225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138700983-C-A

http://identifiers.org/hco/1/GRCh38#19799260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138700946-C-A

http://identifiers.org/hco/1/GRCh38#19799276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138700930-C-A

19799276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138700930-C-G

19799276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138700930-C-T

19799368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700853-A-G

19799368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700853-A-T

19799410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138700831-T-C

19799459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138700785-T-C

19799570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138700705-G-A

19799904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138700546-G-A

19799904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138700546-G-C

19799906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138700544-T-C

http://identifiers.org/hco/1/GRCh38#19799929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138700521-C-A

19799929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non coding transcript exon variant
orthologous variants: 138700521-C-T

19799932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27393
most severe consequence: non coding transcript exon variant
orthologous variants: 138700518-C-T